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1.
Peak activities of radiocaesium (137Cs) in lake sediments have frequently been used to infer the ages of sediments deposited in the 1960s (137Cs derived from nuclear bomb testing) or in 1986 (Chernobyl derived 137Cs). Records of the vertical distribution of 137Cs in sediments can thus be used to provide accurate dates for a critical period in which palaeoecological reconstructions often overlap contemporary monitoring data. However, knowledge regarding how the distribution of 137Cs in sediments is affected by post‐depositional processes is limited to interpretations based on the 137Cs distribution in sediments sampled at a single given date. This study assesses the extent to which the 137Cs record in annually laminated (varved) lake sediments is affected by post‐depositional diffusion, using 11 archived sediment cores sampled between 1986 and 2007. The sediment record reveals how Chernobyl 137Cs incorporated into the 1986 varve diffused downwards in the core at a decreasing rate over time, whereas the surface sediments continued to receive inputs of 137Cs mobilized from the catchment soils or lake margin. In spite of these processes, all cores post‐dating the Chernobyl accident had a clear and well‐resolved peak in the 1986 varve, justifying the use of this feature as a fixed chronostratigraphic feature. Because of the very high levels of Chernobyl fallout at this site, downwards migration of Chernobyl 137Cs has, however, completely masked the nuclear weapons 137Cs fallout peak that had been clearly preserved in the 1964 varve of a pre‐Chernobyl core sampled just three weeks before the Chernobyl accident. In consequence, the weapons fallout marker is likely to be of little use for determining 137Cs dates in areas strongly affected by high levels of Chernobyl fallout.  相似文献   

2.
The redistribution of Chernobyl 137Cs within a small drainage basin was studied in the Lokna river basin, Tula region, Central Russia. Sheet erosion on the cultivated part of basin is the main reason for 137Cs horizontal migration. However there is no statistically significant 137Cs redistribution within cultivated field because of relatively low erosion rates. The valley bottom is the main sink of 137Cs, where 73–84% eroded soil is stored. The resulting 137Cs level in the valley bottom is 1.5–2 times that of the initial 137Cs fallout.  相似文献   

3.
Particle mixing rates (DB) calculated from excess 210Pb gradients in sediments of the east equatorial Pacific range from 0.04 to 0.5 cm2/y, with variation of a factor of 3–4 at a single site. Diffusion of the 236Ra daughter 222Rn may affect 210Pb distributions under conditions of slow mixing and low 210Pb flux to the seafloor, as shown by a siliceous ooze-clay core which contained the fallout radionuclides 239,240Pu and 137Cs but no excess 210Pb (relative to 226Ra). There is no clear relationship between 210Pbderived mixing rates and sediment type, accumulation rate or organic carbon flux to the sediments. Comparison of 210Pb mixing rates with those calculated from 239,240Pu and 137Cs distributions reveals better agreement for a pulse input of the fallout radionuclides (DB = 0.03?0.4 cm2/y) than for continuous input at a constant rate (DB = 0.1?1.6 cm2/y), although the Pu and 137Cs data are better fit by the latter model. The agreement may be fortuitous because 239,240Pu and 137Cs appear significantly deeper than 210Pb in at least one core. Tracer separation could be caused by particle size-selective mixing by the benthic fauna or by chemical mobilization. If the fallout radionuclides are scavenged from surface waters by large, organic-rich particles such as fecal pellets, their release and migration may result from decomposition of the carrier in surface sediments. Either a relatively unreactive form of Pu (e.g. oxidized Pu) has been released by this process or a one-dimensional model is inadequate to explain its observed penetration into the sediments. Activity ratios of 239,240Pu137Cs in the sediments decrease with increasing north latitude, and the trend reflects higher fluxes of 239,240Pu near the weapons test site at Christmas Island (2°N). The 239,240Pu137Cs ratios and fluxes to the sediment (assuming constant input) at the siliceous ooze-red clay site are consistent with published sediment trap data from a nearby site. Thus if fallout radionuclide fluxes to the sea floor were higher in the past, both 239,240Pu and 137Cs have been released from sinking particles.  相似文献   

4.
The collection of large volumes of pore water (1–2 liters per 2 cm horizon of sediment) and low level radiochemical measurements of 239,240Pu and 137Cs have been combined to produce the first study of these fallout artificial radionuclides in marine pore waters. Profiles from box cores taken in June and September 1982 from Buzzards Bay, Mass., are reported along with profiles of many diagenetic constituents (i.e. SO42?, alkalinity, Fe, Mn, DOC, and nutrients).The 239,240Pu pore water profile is characterized by a subsurface maximum of about 0.28 dpm/100 kg lying between 3–11 cm. Overlying seawater, in contrast, has an activity of 0.01 ± 0.02 dpm/100 kg. Below about 11 cm, the pore water 239,240Pu distribution follows that of the solid phase which decreases rapidly with depth. The pore water profiles of 137Cs are characterized by a broad and deeply penetrating maximum where activities of about 35–40 dpm/100 kg extend from 3 to 20 cm. Overlying seawater, in contrast, has an activity of 17–24 dpm/100 kg. The 137Cs and 239,240Pu pore water data show that there is preferential downward transport of 137Cs and that 239,240Pu does not have an active diagenetic chemistry and is not significantly mobile in these coastal sediments.  相似文献   

5.
《Applied Geochemistry》1993,8(5):437-445
The input of137Cs into the troposphere from the Chernobyl nuclear accident made intriguing the use of fallout137Cs as a tool for estimating the rate of soil erosion over Europe. The present paper reports on the adoption of137Cs/134Cs activity ratio to differentiate the vertical distribution of137Cs prioir to and following the Chernobyl accident. The137Cs/134Cs activity ration in the radioactive clouds is required to calculate pre and post- 1986137Cs amounts, considering that the whole134Cs was actually derived from Chernobyl. By using this procedure, the erosion rates could be evaluated for the badland area, the Paglia River basin (central Italy), before and after the Chernobyl accident. Nine sites from two areas of this basin were sampled and analyzed. Erosion rates, ranging from 1.5 to 8.4 mm/a were measured, the values depending both on the basin lithology and site slope. These first results are consistent with those yielded by quantitative geomorphologic methods.  相似文献   

6.
This paper presents a detailed survey of the activities of selected man-made radionuclides in peat deposits located in SW Spitsbergen. Peat cores from the High Arctic (SW Spitsbergen) were analyzed by gamma spectrometry (137Cs), alpha spectrometry (238Pu, 239,240Pu, 241Am activities) and by ICPMS (240Pu/239Pu atom ratios). Maximum activities evident in the peats correspond to the 1963/1964 global maximum fallout from atmospheric testing of nuclear weapons; some of the activity profiles have been altered post-deposition by water infiltration. Activity ratios of 238Pu/239+240Pu, 241Am/239+240Pu, 239+240Pu/137Cs and 240Pu/239Pu atom ratios indicate mixing between global (stratospheric) and regional (tropospheric) sources of these radionuclides in the Svalbard area. The 238Pu/239+240Pu activity ratios varied from 0.02 ± 0.01 to 0.09 ± 0.03, suggesting global fallout as the dominant source of Pu. The 239+240Pu/137Cs activity ratios varied from 0.01 ± 0.01 to 0.42 ± 0.11, which apparently arises from the post-depositional mobility of 137Cs. The 241Am/239+240Pu activity ratios ranged between 0.10 ± 0.02 and 1.5 ± 0.3 and exceed the published global fallout ratio for Svalbard of 0.37 due to the relatively higher geochemical mobility of Pu vs. Am and/or ingrowth of Am from the decay of 241Pu. The atom ratio 240Pu/239Pu ranged from 0.142 ± 0.006 to 0.241 ± 0.027; however, the vast majority of peat samples exhibited 240Pu/239Pu atom ratios similar to the stratospheric fallout (∼0.18).  相似文献   

7.
Continental shelf sediments from nine locations off Washington and Oregon have 239,240Pu inventories which average 8.0 ± 2.6 mCi/km2. The Columbia River and seawaters advecting over the shelf supply Pu which is removed to underlying sediments, principally through scavenging by inorganic paniculate matter. Mass balance calculations argue that less than 20 percent of the advected Pu need be scavenged from the water column to balance river input and total shelf sediment inventories. The percentage of the Pu removed through scavenging is consistent with observed participate concentrations in shelf waters and published sediment/water distribution coefficients.No marked separation of Pu from 137Cs is observed with depth in Pacific shelf sediments as has been reported in Atlantic coastal sediments. This interocean distinctness can be explained by differences in particle mixing and downward diffusion of Cs in sediments of varying porosities. The transuranic inventories and Pu/Cs ratios in the Pacific sediments do not support the hypothesis of Livingston and Bowen that Pu is remobilized within the sediment column by ‘complexone’ formation with (principally) organic substances.Excess 210Pb/239,240Pu inventory ratios in eight representative cores from the Washington shelf average 100 ± 19, even though absolute values of both inventories vary by much larger factors. This reasonably constant ratio, for a given water depth, permits estimation of total Pu inventories and prediction of sites of unusual Pu accumulation from data on the more easily measured natural radionuclide.  相似文献   

8.
Isotopes of plutonium (Pu), cesium (Cs), and cobalt (Co) introduced into the Hudson River Estuary from fallout deposition, the erosion of fallout-contaminated surface soils, and nuclear reactor effluent (isotopes of Cs and Co only) have been measured in water column samples collected from 1975 to 1980 Isotopic measurements conducted independently by two research groups utilizing different sampling and analytical techniques have been summarized. The major conclusions drawn from the work are that for water samples collected by the two laboratories over similar time periods, the mean concentrations of nonfilterable239,240Pu (<0.45 μm) were identical at 0.13 fCi/l, mean concentrations of both137Cs and239,240Pu in suspended particulates were more divergent at 2,270±920 pCi/kg (±1 SD) and 1,430±430 pCi/kg for137Cs, and 19±8 pCi/kg and 12±4 pCi/kg for239,240Pu The behavior of239,240Pu and137Cs within the water column is shown to diverge within brackish waters Specifically, the magnitude of the137Cs distribution coefficient (K d ) can be expressed as an inverse power function of the chloride ion concentrations for chlorinities between 0.1 and 4 g Cl−/l No difference in the239,240PuK d has been observed between fresh and brackish waters Based on the expected inventories of239,240Pu and137Cs within watershed soils, the current downstream transport of these radionuclides represents fractional mobilization rates on the order of 1–4 (×10−4) per year  相似文献   

9.
Single cores from two salt marshes in the United Kingdom located near different nuclear facilities were investigated to compare chronostratigraphic estimates derived from the natural radionuclide 210Pbexcess with estimates from the known times of introduction of artificial radionuclides to the environment. Both cores selected had clear visual indications of redox zonation, and evidence for diagenetic redox perturbation of the radionuclide records was also sought. In the core from Beaulieu Marsh on the south coast of England, the redox zonation was revealed by the profiles of the redox-sensitive elements Mn + I, Fe + P + As, and S, and the records of nuclear discharges were entirely contained within oxidized conditions in the upper 40 cm. The constant flux/constant sedimentation 210Pbexcess accumulation estimate was 76% of that derived from the 1963 fallout 137Cs level (0.35 vs. 0.46 g cm−2 yr−1 dry mass), but the constant flux 210Pbexcess method indicated that accumulation rates were lower at Beaulieu before ∼1950. On any timescale, 137Cs appears earlier in the sediment record than its introduction to the environment, but although downward diffusion of 137Cs relative to 241Am has clearly occurred, the 137Cs peak still appeared in place and there was negligible penetration of 137Cs into underlying reduced conditions. This core also contained a peak of the 60Co discharges from either or both the Winfrith and La Hague nuclear plants that peaked in 1980 and 1984, respectively. The sediments in the core from Wyre Marsh on the eastern coast of the Irish Sea had accumulated more rapidly than those at Beaulieu, and in this case the redox zonation could be established only from Mn and S profiles. Here, the constant initial activity 210Pbexcess accumulation rate estimate was 125% of that derived from the 137Cs peak correlated with the 1975 Sellafield discharge maximum (0.79 vs. 0.64 g cm−2 yr−1). Sellafield discharge 137Cs swamps fallout or Chernobyl 137Cs signals in this core, but the 137Cs and 241Am sediment records are well separated and remain consistent with the slightly different discharge patterns over time. This is so despite the fact that the maximum activity levels of both isotopes are now located well into reducing conditions out of which Mn must have migrated. The 210Pb profile appeared similarly unaffected by the oxidized/reduced boundary in this case. This core was too short to define the limits of any downward 137Cs migration. 210Pbexcess accumulation rate estimates for salt marshes should be viewed with some caution because of the steady-state assumptions inherent in all 210Pbexcess methods and the potential for fluctuating accumulation conditions and open system behavior in salt marshes.  相似文献   

10.
The relative mobility of nuclides of Pb, Th, Pu, and Cs, which are widely used as geochemical tracers for sedimentation and bioturbation. was investigated in artificial microcosm tanks (MERL) and in Narragansett Bay. Their mobility was characterized by their removal rates from the water column, their affinity toward particles and their degree of penetration into the surface sediments. Pb, Th, and Pu transport was controlled predominantly by the affinity of these elements to particles, and the transport parameters of the particles themselves (i.e. sediment resuspension and mixing rates). Because of its low distribution coefficient, transport of Cs was controlled by molecular diffusion through pore water in the winter, while in summer, Cs transport was enhanced due to bioturbation. The increase with depth of the CsPu ratio in core profiles of MERL and Narragansett Bay sediments is thus caused primarily by the higher mobility of Cs.  相似文献   

11.
Low reference inventories of the fallout radionuclide 137Cs in low latitudes may limit its present and future application for studies of soil erosion and sediment redistribution in Southeast Asia. 137Cs reference inventories and concentrations in surface materials measured in nine and five areas, respectively, across Southeast Asia are here reported and reviewed. The compiled reference inventories decrease from north to south. Three global estimates of 137Cs total fallout are also reviewed and compared to the measured data while taking into account factors that affect the fallout estimates and the reference inventory. The results are presented as a schematic regional distribution map of 137Cs reference inventories for the year 2012. A relationship between a reference inventory and topsoil concentration is also provided. The measured 137Cs concentrations suggest that a minimum detectable activity (MDA) less than 0.5 Bq/kg is required for detection of 137Cs activity in topsoils in the lowest reference inventory areas. This sensitivity should allow, at present, 137Cs to be a useful tool for analysis of soil erosion in Southeast Asia, should also be a useful chronometer, and will be a useful tracer at least where the reference inventory is more than 500–600 Bq/m2. This level of MDA has been demonstrated in previous studies to be achievable by gamma-ray spectrometry using non-destructive sample treatment. As the nuclide decays, sufficient will remain to be useful until the middle of this century in most areas in Peninsular Malaysia and southern maritime Southeast Asia, and a few decades more in the rest of the region.  相似文献   

12.
Vertical profiles of137Cs and210Pb have been determined in a 9 m column of ice from accumulation zone of Changme-Khangpu glacier in north Sikkim valley.137Cs activity varies from 4 to 22 dpm/ L. In many samples210Pb occurs at a level of 20 to 65 dpm/ L which is much higher than the expected fallout value.137Cs and210Pb activities correlate well with each other but not with the dust content. Possibility of210Pb production in the nuclear explosions is discussed. Several peaks appear in the depth profile of137Cs and210Pb which can be matched with Chinese atmospheric nuclear explosions with some phase difference if a uniform ice accumulation rate of 0.7 m per year is assumed since 1969.  相似文献   

13.
Cores were collected from the length of Pakuranga estuary, a small urban estuary in Auckland, New Zealand, to determine sedimentation and contaminant history, and in particular the impact of urbanization. Catchment sediment loads for the most recent history (1953–1995), including urbanization since 1960, were reconstructed using the landcover history and soil erosion modeling. Pollen and14C dating and pre-urban landcover history were used to reconstruct early estuary sedimentation (i.e., post-3000 yr BP to 1960). Heavy metal concentrations, particle size,137Cs, pollen, and catchment sediment loads were all needed to disentangle the complex estuarine response to urbanization.137Cs profiles did not reflect the historical fallout pattern, but deposition of137Cs-labelled eroded catchment soil, coinciding with peaks in urban construction. Temporal variations in stormwater137Cs concentrations are likely due to varying contributions from137Cs-rich topsoil and137Cs-poor subsoils. A similar pattern was observed in heavy-metal concentrations and attributed to street runoff rather than topsoil being diluted by metal-poor subsoils. Dating of the sediment profiles showed that during urbanization sedimentation rates in the tidal creek and estuary were higher than sedimentation rates associated with past agricultural landuse and the original forest landcover. Urbanization has brought about substantial environmental changes in the upper estuary through continued infilling of shallow, intertidal areas, contamination by heavy metals to levels of ecological concern, sediment textural changes, and rapid mangrove colonization of formerly bare intertidal sediments.  相似文献   

14.
The paper presents results of radiocological monitoring at the site of the Kraton-3 accidental underground nuclear test in Yakutia. The distribution and migration of 137Cs, 90Sr, 237Np, and 238–240Pu in the soil and its living cover of the northern taiga are analyzed, and it is demonstrated that the radioecological conditions at the territory are still adverse in spite of the rehabilitation measures.  相似文献   

15.
Four overbank sediment profiles in the Inari area of northern Finnish Lapland were studied in detail by the collection of samples at one-centimetre intervals. The sample sites are situated along a line from northeast to southwest away from the industrial centre at Nikel in the Kola Peninsula. Total, aqua regia and ammonium acetate leachable concentrations were determined for more than 30 elements to study their vertical distribution, and to evaluate the results of the three analytical methods in environmental studies. Radioisotopes of 137Cs and 134Cs were measured on 34 samples to assess radioactive fallout. Radiometrie 14C-dating was determined in one profile to estimate the rate of sedimentation. Grain-size analysis was carried out for calculating the field weight to produce a minimum of 500 g of minus 125 μm material, required for analysis and storage, and to estimate the clay content, which affects leachable element concentrations, when partial or near-total analytical methods are used.It was found that the concentration of studied elements varies with depth. Airborne Ni and S contamination from the smelting plants in the Kola Peninsula was weakly detectable by ammonium acetate leachable contents.137Cs and 134 Cs isotope concentrations, originating from the nuclear weapon tests on the island of Novaya Zemlya and/or from the Chernobyl nuclear power plant accident, were clearly detectable in the topmost layer of overbank sediments. 14C dating has given a time-lag of 5000 years for the deposition of an overbank sediment sequence of 120 cm thickness. Thus, a very slow deposition rate of overbank sediments in northern Finnish Lapland is indicated.It is concluded that grain-size analysis and radiometric dating are necessary for a full interpretation of the geochemistry of overbank sediment sequences, and the selection of leaching methods should be done according to the character of the assumed contamination.  相似文献   

16.
In Russia, until recently, it was considered that groundwater was protected from surface radioactive contamination by soil and rocks in the zone aeration. Groundwater was not a subject of radiation control. The accident at the Chernobyl Nuclear Power Plant showed, however, that groundwater is vulnerable to radioactive contamination. In this connection, the vulnerability of groundwater to and the problems of protecting groundwater from radioactive contamination became urgent. The assessment of natural protection of groundwater from radioactive contamination is now considered a top priority. The zone of aeration is generally considered to be the zone separating groundwater from surface contamination. In respect to radioactive contamination, soils that may fix a large quantity of radionuclides serve as a protection zone of a higher order. The mapping of protectibility was done for each radionuclide taking into consideration the specific structure of the flow medium and migration properties of a radionuclide.90Sr and137Cs have different mechanisms of transport; convective transport is characteristic of the former and diffusive transfer of the latter. This is conditioned by different physico-chemical properties of the radionuclides and principally by their sorption capacities. The coefficient of distribution of90Sr is in many times less than the coefficient of distribution of137Cs. The environmental protection problem in regions with nuclear power plants and in areas subjected to radioactive contamination may be solved using a monitoring, system including interrelated systems of observation and prediction of the lithosphere and the hydrosphere. The problem of mathematical modeling of migration processes is related to the complexities of modeling the processes of flow, mass transfer, and the accompanying physicochemical processes in zones of full and partial saturation, as well as difficulties in mathematical calculations.  相似文献   

17.
The formulation of watershed management strategies to protect water resources threatened by soil erosion and sedimentation requires a thorough understanding of sediment sources and factors that drive soil movement in the watershed. This paper describes a study of medium-term water-driven soil erosion rates in a mountainous watershed of the Shihmen Reservoir in Taiwan. A total of 60 sampling sites were selected along a hillslope. At each sampling site, the inventory 137Cs activity was determined and then calculated with the diffusion and migration model to derive soil erosion rates. The rates are one to two orders of magnitude lower than estimates using the Universal Soil Loss Equation, a soil erosion model often used in Taiwan. Results of multiple regression analysis indicate that the spatial variability of soil erosion rates is associated with the relative position of a sampling site to the nearest ridge and soil bulk densities (r 2 = 0.33, p < 0.01). Finally, the patterns of soil redistribution rates on the hillslope follow the 137Cs hillslope model as soil erosion increases in the downslope direction. No deposition site is found at footslope because soil deposition is swept away by regular flooding along the stream channel. This study is an important first step in using 137Cs as a tracer of soil redistribution in mountainous watersheds of Taiwan.  相似文献   

18.
Nuclear facilities in coastal locations often discharge low‐level liquid wastes into the sea and the radioisotopes in these discharges are of interest both in assessing possible environmental impacts and as tracers for coastal processes. The distributions of a range of artificial radionuclides, derived from the authorized discharges from British Nuclear Fuels (BNFL) Sellafield, have been determined in the sediments of an intertidal salt marsh in the Esk Estuary, Cumbria, UK. Where published discharge histories exist (for 137Cs, 238Pu, 239,240Pu and 241Am), the sediment core‐profile distributions of these radionuclides have been compared with the releases from Sellafield, and consistent values of the accumulation rate (0·226 ± 0·007 g cm?2 yr?1) are obtained. A quantitative model has been developed, describing association of radionuclides with suspended particulate material, which is then accumulated and mixed in an offshore mud patch before resuspension and deposition in the salt marsh. The model has been used to describe radionuclide distributions observed in both the mud patch and the salt marsh, and to identify isotopes for which post‐depositional remobilization or solution transport from the discharge point are important. The behaviour of the commonly studied isotopes (137Cs, 238Pu, 239,240Pu and 241Am) is similar to that observed at this and other nearby locations. The activation product isotope 236U is enhanced in these sediments over the natural baseline by four to eight orders of magnitude, and the results suggest that Sellafield‐derived uranium is comparably mobile to 137Cs in these sediments although the processes governing the behaviour of these two elements may be different. In situ production of 241Am by decay of its 241Pu parent has generated only 17% of the current sediment inventory of this isotope, insufficient to account for the increase over the last 20–25 years, and suggesting that the input material for these sediments is preferentially enriched in Am relative to Pu during transport from the offshore mud patch. The discharge history of 244Cm, which is unknown, has also been reconstructed from the sediment profile and the model.  相似文献   

19.
 Surface contamination with radioactive caesium introduced into the environment after the accident at the Chernobyl nuclear plant was high enough in the Crimean Mountains to allow using radiocaesium as an indicator of penetration of radioactive contamination into a karst system. Caesium concentrations have been studied in soils above Marble Cave, Tchatyrdag Plateau, in percolation waters and in sediments transported by percolation waters within the cave. Contamination of the daylight surface with 137Cs is about 30 kqB m–2 which is approximately 13 times higher than the density of global fallouts. Besides 137Cs, almost all samples showed presence of 134Cs with the 137Cs/134Cs ratio close to that of Chernobyl contaminations. Concentrations of 137Cs range from 9 to 15 mBq l–1 in the present percolation waters in the cave. In sediments related to percolation waters 134Cs is detected in some samples besides 137Cs, although the effect of 228Ac is not ruled out. Surprisingly, the highest concentrations of radiocaesium were measured in "old" sediments in the cave's lower series. These sediments are not associated with modern percolation and are represented by a clay/moonmilk alternating sequence deposited in an old dried cave lake. Moonmilk layers have higher caesium content than clay. It is assumed that Chernobyl caesium was transported into the cave with aerosols which were then deposited mainly in areas where condensation occurs. The sampling site is located just in the boundary between two microclimatic zones with a temperature gradient of 0.5  °C. Active condensation processes occur in this area. Caesium was not detected in another similar sampling site (old lake deposits) located within homogeneous microclimatic conditions. If the above interpretation is correct, these results show the geochemical significance of the aerosol-condensation mechanism of mass transport and localisation. Received: 1 June 1995 · Accepted: 4 December 1995  相似文献   

20.
This paper describes the use of 210Pb and 137Cs radioactivity measurements to determine the rates of sedimentation in the Great Lakes. Cores from eight locations in Lake Michigan were chosen for examination to cover as wide as possible a range of sedimentation rates and representative sedimentary environments. The surficial 210Pb activity in the sediments varies between 7 and 23 pCi/g dry wt and its profile in each core shows the expected exponential decrease with depth consistent with the assumption of uniform sedimentation rate over the last hundred years and secular equilibrium between supported 210Pb and 226Ra (0.5-1.0 pCi/g dry wt). Companion measurements of 137Cs indicate that the coring technique satisfactorily recovered the uppermost levels of the deposit and that the mobility of both radionuclides within the sediment is probably small.Based on the limited number of cores analyzed to date, it appears that modern sedimentation rates are not very different from average rates for the last 7000 yr. The excess 210Pb appears to originate primarily from atmospheric fallout, but a further inventory of the 210Pb distribution over the lake bottom must be made to properly assess the significance of other sources. The spatial distributions of both 137Cs and 210Pb at certain stations suggest that the mode of transport of these radionuclides are comparable and involve attachment to settling particles. A mathematical model is developed which accounts for the observed limited mobility of both 210Pb and 137Cs in several of the cores in terms of post-depositional redistribution by physical or biological mixing processes.  相似文献   

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