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1.
The moment magnitude (M w) 9.0 Tohoku-Oki Earthquake occurred on March 11, 2011, generating an unusually large tsunami. The seismic shocks and tsunami inundation severely damaged the Fukushima Daiichi Nuclear Power Plant. Radionuclide emission due to reactor breakdown contaminated wide areas of Fukushima and its surroundings. Heavy rainfall causes runoff across surface soil, and fine soil particles are susceptible to uptake by the flowing water. The high radioactivity of grains suspended in floodwater indicates that radioactive fallout was streamed into rivers in particulate form and transported downstream under high-flow conditions. Here, we investigated the diachronic mode of 134Cs and 137Cs in central Fukushima, through which the contaminated air mass drifted and caused wet deposition of radionuclides. Stratigraphic measurements of radioactivity in sediment cores is the method employed in this study to determine the basin-wide movement of 134Cs and 137Cs, to evaluate the significance of the erosion–transportation–accumulation processes on natural decontamination in terrain characterized by steep slopes and high precipitation. Stratigraphic results illustrate the process of fluvial sediment discharge, and the massive deposition of radiocaesium suggests basin-wide movement of fallout during concentrated rainfall. Grain suspension in torrential currents is an important pathway for transportation of radionuclides from land to sea, and the appearance of hotspots on floodplains and the offshore sea floor is the consequence of erosion and transportation under seasonal heavy precipitation. Radioactive horizons occur in offshore sediment columns and thus radiocaesium discharged from the estuary will persist forever under the sea floor if no artificial disturbance occurs.  相似文献   

2.
Adsorption of trace amounts of radiocaesium on NH4-, K-, and Na-saturated Fithian illite and subsequent desorption by 1 M NH4 showed that a substantial amount of radiocaesium (44%, 46%, and 91% for NH4-, K-, and Na-illite, respectively) cannot be desorbed after only 5 min of adsorption. Our results suggest that this instantaneous fixation is caused by the collapse of the frayed edges of the clay mineral and the relatively high concentration of radiocaesium building up in solution in the batch desorption experiments. Consequently, commonly applied high-NH4 extractions underestimate truly exchangeable amounts of radiocaesium in soils and sediments containing illitic clay minerals. The rate of desorption of trace amounts of radiocaesium from the solids using high NH4 or Cs concentrations has a half-life of about 2 yr, reflecting radiocaesium desorption from (partially) collapsed interlayers. Extraction of radiocaesium from illite after 5 min of contact time with a Cs-selective adsorbent or a 1 × 10-6 M CsCl solution shows that 100% of the bound radiocaesium is readily available. The desorption rate in the presence of a Cs-selective adsorbent has a half-life of about 0.2 yr. Desorption of radiocaesium from illite using different ammonium concentrations shows that radiocaesium partitioning follows reversible ion-exchange theory if the NH4 concentration is below 1 × 10-4 M, and sufficient time (weeks) is allowed for the reaction to proceed. Thus, radiocaesium sorption reversibility in the natural environment is much higher than generally assumed, and equilibrium solid/liquid partitioning may be assumed for the long-term modelling of radiocaesium mobility in the natural environment. In the particular case of anoxic freshwater sediments with very high NH4 concentrations in the pore waters (up to several mmol.L-1), collapse of the frayed edges of illite may occur, influencing radiocaesium partitioning. If collapse occurs before radiocaesium adsorbs to illite, high caesium sorption reversibility as measured by high-NH4 extraction can be expected because further collapse of the frayed edges during the extraction procedure will be limited. This effect has indeed been observed earlier in the extraction of radiocaesium from anoxic freshwater sediments with high-NH4 solutions and was as yet unexplained.  相似文献   

3.
《Applied Geochemistry》1996,11(4):601-603
An equation is presented for predicting solid/liquid distribution coefficients of radiocaesium on soils and sediments (freshwater and marine). The equation is based on the value of the radiocaesium interception potential of the illitic frayed edge sites of the system and liquid phase composition (K, NH4 and Na). The predictive potential of the equation is tested for some 130 combinations of soil/sediment and water composition covering a three-order-of-magnitude range in KD137Cs values. On average, experimental KD137Cs values exceed predicted values by a factor of 1.62 ± 0.75.  相似文献   

4.
Sources of input contributing to the organic matter of four different Mediterranean sapropels (S1, S5, S6, S7) are inferred from the relative distributions of terrigenous and marine biological markers in these Quaternary deposits. The relative terrigenous contribution does not vary significantly. Within the marine contribution there is a significant compositional variation. A contribution from dinoflagellates is relatively important in the S1 sapropel, whereas sapropels S6 and S7 are characterized by a relatively large contribution from prymnesiophyte algae and planktonic cyanobacteria. The abundance of diatoms in sapropel S5, as deduced from microscopic observations, is probably reflected by a high concentration of loliolide.Variations in sea-surface water temperatures can be deduced from the relative abundance of di- and triunsaturated C37 ketones (Uk37 index) and from the relative abundance of esterified 27-nor-24-methylcholesta-5,22E-dien-3β-ol and cholesta-5,22E-dien-3β-ol (STI index). These two molecular temperature indices are consistent with the δ18O record and with the pollen record of the sapropels investigated.  相似文献   

5.
Analysis of the molecular composition of the organic matter (OM) from whole sediment samples can avoid analytical bias that might result from isolation of components from the sediment matrix, but has its own analytical challenges. We evaluated the use of GC × GC-ToFMS to analyze the pyrolysis products of six whole sediment samples obtained from above, within and below a 1 million year old OM-rich Mediterranean sapropel layer. We found differences in pyrolysis products <n-C22 between the OM-rich sapropel samples and the OM-poor background marls. The presence of alkyl pyrroles, probably derived from chlorophyll, in pyrolysates of the sapropels but not in those of the marls suggests that higher marine productivity and greater OM preservation accompanied deposition of the sapropels. Detection of tetramethyl benzenes considered to be pyrolysis products of isorenieratene in the sapropel samples is evidence that nitrogen-fixing green sulfur bacteria contributed to the high productivity. Greater abundances of shorter chain aliphatic hydrocarbons, pyrroles, furans and alkyl aromatics in the pyrolysates of sapropel samples relative to the marls confirm better preservation of marine OM in the sapropels. In addition, the presence of greater amounts of thiophenes in the sapropels than in the marls is consistent with the existence of euxinic conditions during sapropel deposition. The combination of whole sediment pyrolysis and GC × GC-ToFMS is promising, but the procedure requires careful selection of its multiple analytical variables, particularly the pyrolysis temperature and the operational features of the GC columns.  相似文献   

6.
Organogenic sediments (sapropels) in lakes are characterized by a reduced type of diagenesis, during which organic compounds are decomposed, the chemical composition of the pore waters is modified, and authigenic minerals (first of all, pyrite) are formed. Pyrolysis data indicate that organic matter undergoes radical transformatons already in the uppermost sapropel layers, and the composition of this organic matter is principally different from the composition of the organic matter of the its producers. The sapropels contain kerogen, whose macromolecular structure starts to develop during the very early stages of diagenesis, in the horizon of unconsolidated sediment (0–5 cm). The main role in the diagenetic transformations of organic matter in sediments is played by various physiological groups of microorganisms, first of all, heterotrophic, which amonifying, and sulfate-reducing bacteria. SO42? and Fe2+ concentrations in the pore waters of the sediments are determined to decrease (because of bacterial sulfate reduction), while concentrations of reduced Fe and S species (pyrite) in the solid phase of the sediment, conversely, increase. Comparative analysis shows that, unlike sapropels in lakes in the Baikal area, sapropels in southern West Siberia are affected by more active sulfate reduction, which can depend on both the composition of the organic matter and the SO42? concentration in the pore waters.  相似文献   

7.
The Holocene successions of numerous shallow lakes located along the Coorong coastal plain in South Australia attest to the impact of rising sea level and changing climate on their depositional environment. Old Man Lake is one of the smallest perennial alkaline lakes in the region. Its succession comprises a basal lagoonal sand rich in humic organic matter (OM) overlain by a 3.7 m thick upward shoaling lacustrine mudstone. The latter features three discrete sapropel units deposited between 3270 and 4910 cal yr BP, a time of increasing aridity throughout southeastern Australia. A core taken from the lake’s eastern margin yielded sedimentological, mineralogical, geochronological and micropaleontological data. Coring at five other sites across the lake provided sections of the humic and sapropelic facies (n = 20) for total organic carbon and Rock–Eval analysis; isotopic characterization of their micritic carbonate (δ13Ccarb, δ18Ocarb) and co-existing OM (δ13Corg); and GC–MS and GC–irMS analysis of their free aliphatic hydrocarbons. For each ‘sapropel event’ high productivity of diatoms and green algae was the principal driver of the accumulation and preservation of OM in such high concentrations. The precursor algal blooms were likely triggered by the influx of fresh water following winter rainfall. The combination of kerogen hydrogen index and δ13Ccarb–δ13Corg, previously employed to track secular changes in algal productivity and organic preservation, proved useful in identifying synchronous geographic differences in these processes across the lake. Highly branched isoprenoids (HBI: C25:1 ≫ C20:0) are prominent components of the aliphatic hydrocarbons in the sapropels, confirming the significant contribution of diatoms to their OM. The C isotopic signatures of the principal C25:1 HBI isomer and the co-occurring C23–C31 odd carbon numbered n-alkanes further document the non-uniformity of biomass preservation within and between the three sapropel units. The evidence from this study suggests that seasonal algal blooms and meromixis, although not necessarily an anoxic hypoliminion, were required for sapropel formation in the Holocene lakes of the Coorong region. Higher resolution sampling, dating and comparative analysis (microfossil, biomarker and isotopic) of these sapropels is required to clarify their potential significance as palaeoclimate proxies.  相似文献   

8.
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9.
《Applied Geochemistry》1998,13(7):803-814
The Chernobyl radionuclides distribution and mobility in soils and uptake by plants have been studied in seminatural and agricultural moraine and in fluvioglacial landscapes typical for the areas of the Bryansk region affected by the accident.The major part of the Chernobyl 137Cs accumulated in the topsoil is insoluble in water, 40 to 93% of this radionuclide is strongly fixed by soil, while 70 to 90% of the 90Sr is present in water soluble, exchangeable and weak-acid soluble forms. Radionuclide vertical migration is most pronounced in local depressions with organic and gley soils in which both radionuclides are detected to the depth of 30–40 cm.In woodlands, most of the 137Cs is still fixed in litter and the upper mineral soil layer. The concentration peak in litter has moved to the lower AOF layer. Concentration in topsoil leads to high radionuclide uptake by forest species with shallow root systems (bilberry, mushrooms, fern). Contaminated forest products may contribute considerably to the internal irradiation doses of the local population. On flood plain grasslands traditionally used by local populations for haycrops and grazing, radionuclides are more strongly fixed in soils with fine texture. Radioisotope uptake by plants decreases in the order: legumes>herbs>grasses. Transfer to grasses in local depressions is usually higher compared with the dry levees. Observed exclusions are assumed to be due to comparatively low mobility of 137Cs and relatively high K content in soil. 137Cs accumulation in potato tubers grown on sandy soddy podzolic watershed soils mainly corresponds to its total amount in soils; uptake of 90Sr depends upon the percentage of its most mobile fraction.Pronounced relief is proved to cause different patterns in distribution and migration of radionuclides in soils and local food chains. The study showed it to be true for private farms situated in different landscape positions within the same settlement.The forest litter, topsoil and products, and flood plain pastures, especially localities in depressions are critical materials for the long-term radioecological monitoring of the contaminated landscapes of the study area and those of similar conditions. Population of the areas within the zone of contamination exceeding 15Ci/km2 (555kBq/m2) should be recommended to exclude local forest products from their diets and to avoid cattle grazing on wet flood plain meadows without remediation.  相似文献   

10.
The δ13C values of higher plant wax C27–33 n-alkanes were determined in three, time-equivalent Pliocene (2.943 Ma) sapropels and homogeneous calcareous ooze from three different sites forming an east-west transect in the eastern Mediterranean Basin in order to study the composition of the vegetation on the continents surrounding the Mediterranean Sea. A two-end member mixing model transformed the measured δ13C values into the contribution of C4 plants to the terrestrial vegetation. These calculations indicated a high C4 plant contribution (i.e. 40–50%) in the periods just before and just after sapropel formation. During sapropel deposition the C4 plant contribution increased by up to 20% at all sites. This is interpreted to record the increased overall plant coverage of the Mediterranean borderlands resulting from the change in formerly barren desert areas into C4 grass-dominated savannahs as a response to the wetter climate during sapropel deposition. Enhanced accumulation rates (ARs) of long-chain n-alkanes (C27–33) and n-alkan-1-ols (C26–30) towards the middle of the sapropel in concert with a decrease in the Ti/Al ratio confirm an increased delivery of terrigenous organic matter at all sites. These biomarkers were probably predominantly fluvially transported to the Mediterranean Sea, not only by the Nile but by fossil wadi river systems on the northern African continent.  相似文献   

11.
The biogeochemistry of organic lacustrine sediments (sapropels) has been poorly studied in Siberia. In this paper we show the specifics of sapropel formation caused by low pH and mineralization of water by the example of Lake Ochki in Cisbaikalia. The main sources of organic matter are zoo- and phytoplankton, which concentrate mostly basic chemical elements and also some alkaline, alkali-earth, and chalcophile elements and move them to the sediment. The calculated enrichment factors (EF) have shown that the lake plankton is strongly enriched with phosphorus and chalcophile elements. The calculations have also revealed a great contribution of the plankton to the elemental composition of sapropel (Mebio, %): P (-100), Cd (57), Br (45), Hg (40), Se and Na (30), Zn (23), K (21), and Ca (15). Elements are rather uniformly distributed throughout the 3.2 m thick sapropel layer. Lithophile elements (Al, Sc, Ti, Y, Zr, Nb) and LREE are mostly from a terrigenous source. The high contents of mobile elements (Cd, Sb, Sn, Pb, Zn) in the upper part of sapropel are probably due to anthropogenic factors. The high Cu and Zn contents in some sapropel layers are probably related to the inflow of deep-level groundwaters, and the elevated contents of Hg, Cd, and Sb might have been caused by forest fires.  相似文献   

12.
Consideration of the impact of substantial changes in soil temperature or moisture regime on the geochemical forms of radionuclides is important for more accurate assessment of the environmental risk posed by radionuclide migration and potential biological availability, especially in the first months after their release into the environment. This paper presents the results from a study of the influence of cooling, freezing and soil drought on the migration and potential bioavailability of 60Co and 137Cs in two soils (a fluvisol and a cambisol, according to the World Reference Base for Soil Resources/FAO) from Bulgaria. The changes in the geochemical fractionation of 60Co, the exchangeable 137Cs and water-soluble forms of both radionuclides were examined under different storage conditions up to 5 months after their introduction into the soils in solution form. Freezing or soil drought resulted in a significant increase of the water-soluble forms of 60Co in the fluvisol soil, defining higher mobility and potential bioavailability. No influence of the storing conditions on the water-solubility of 60Co in the cambisol soil was established. The cooling, freezing and soil drought caused an increase of the exchangeable 137Cs in both soils.  相似文献   

13.
 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   

14.
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   

15.
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   

16.
Cesium and Strontium concentrations were analyzed in eight pedogenetic soil profiles developed on different rocks from a semiarid mediterranean region: La Mancha (Central Spain). Concentration activities of 137Cs and 90Sr, as for some soil properties, were also measured. The results are presented in this document: Cs concentrations range between 0.4 and 18.3 mg kg−1 and Sr varies widely between 11.0 and 3,384 mg kg−1. Therefore, it is clear that there is a broad range of concentrations and there are also values significantly higher than the average values stated by several authors. Concentrations of long-life artificial radionuclides (137Cs, 90Sr) were determined in some of the same soils. The activity concentration mean values (Bq kg−1) were ranging between 0.82 and 21.76 for 137Cs and 90Sr variations range between 6.73 and 0.35. There were no significant correlations between radionuclides and stable trace elements. The data indicate that the soils do not show significant radioactivity of these elements and therefore they do not pose a danger. By the same token, no risk of contamination by this activity was detected. Finally, spatial patterns seem to be affected by the soil type and some soil properties.  相似文献   

17.
The oxygen and carbon stable isotope compositions of cave speleothems provide a powerful method for understanding continental climate change. Here, we examine the question of the regionality of this isotopic record and its linkage with the marine isotopic record in the Eastern Mediterranean (EM) region. The study presents a new, accurately dated 250-kyr δ18O and δ13C record determined from speleothems of the Peqiin Cave, Northern Israel. Its comparison with the continuous 185-kyr isotopic record of the Soreq Cave speleothems from Central Israel reveals striking similarities. Thus, a strong regional climatic signal, brought about by variations in temperature and rainfall amount, is reflected in both cave records. Low δ18O minima in the Peqiin profile for the last 250- to 185-kyr period (interglacial marine isotopic stage 7) match the timing of sapropels 9 to 7 and are indicative of high rainfall in the EM region at these times. The combined Soreq and Peqiin δ18O record for the last 250 kyr excellently matches the published Globigerinoides ruber (G. ruber) marine δ18O record for the EM Sea, with the isotopic compositional difference ΔG.ruber-speleothems remaining relatively constant at −5.6 ± 0.7‰, thus establishing for the first time a robust, exploitable link between the land and the marine isotopic records. The correspondence of low δ18O speleothem values and high cave water stands with low G. ruber δ18O values during interglacial sapropel events indicates that these periods were characterized by enhanced rainfall in the EM land and sea regions. By use of sea surface temperatures derived from alkenone data as a proxy for land temperatures at the Soreq Cave, we calculate the paleorainfall δ18O values and its amounts. Maximum rainfall and lowest temperature conditions occurred at the beginning of the sapropel events and were followed by decrease in rainfall and increase in temperatures, leading to arid conditions. The record for the last 7000 yr shows a trend toward increasing aridity and agrees well with climatic and archeological data from North Africa and the Middle East.  相似文献   

18.
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   

19.
Geochemical studies of the ecosystems of 184 Siberian lakes in three largest zones of northern Asia (humid, arid, and semiarid) and in mountainous area were carried out. The contents of natural radionuclides, radiocesium, and rare-earth elements in conjugate components of the systems and the types of the main sources of the bottom sediment material have been determined.Dating of the bottom sediments was made by the activity of radioisotopes 137Cs and 210Pb, which permitted estimation of the sedimentation rates in lakes in different regions of Siberia: 0.35 cm/year in the south and 0.25–0.3 cm/year in the north.Six main ions have been determined in the waters of the studied lakes: Ca2+, Mg2+, Na+, HCO3?, SO42?, and Cl?. The distribution of natural radionuclides in the stratified sections of bottom sediments of Siberian lakes evidences the stable sedimentation and characterizes their contents in the soils of water-catchment areas, which can be considered background contents there. Sediments enriched in organic matter have higher concentrations of U and lower ones of Th and K. The Th/K ratio in the studied bottom sediments is the same as in the soils. The Th/U ratios are somewhat lower than those in the soils because U is accumulated by chemogenic and organic components. The overall 137Cs pollution of bottom sediments of Siberian lakes is close to the global background (40 mCi /km2 in 2000), but in the Altai Territory and Buryatia and Altai Republics it is twice higher. The uneven areal and temporal distribution of residual radiocesium is observed not only in the lacustrine sediments but also in the lake water areas. The REE patterns of bottom sediments of different mineral types are similar to those of continental crust and clays of the Russian Platform, though organogenic and carbonate sediments have higher absolute REE contents than terrigenous ones. Pelitic fraction is the main REE concentrator in the bottom sediments.  相似文献   

20.
The paper presents data on sapropels from ten lacustrine systems at the Barabinsk and Kulunda plains in Novosibirsk region. The sapropels are classified according to the type of the biological contribution to their origin and the content of organic matter. The sapropel of lakes Kachkulnya and Barchin, which are rich in organic matter and differ by the type of their origin (macrophytogenic and planktonogenic), were studied in much detail with the application of the following techniques: X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), and elemental (CHNSO) analysis. Groups of organic compounds contained in the organic matter were determined by successive extraction, and the monosaccharide composition was studied by high-performance liquid chromatography (HPLC). The organic matter of sapropel with different type of boilogical contribution was discovered to differ in elemental (CHNSO) composition, group of organics, and the monosaccharide compositions. Our results led us to conclude that the genesis of sapropel significnalty imprints the composition of its organic matter.  相似文献   

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