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1.
Playa systems are driven by evaporation processes, yet the mechanisms by which evaporation occurs through playa salt crusts are still poorly understood. In this study we examine playa evaporation as it relates to land surface energy fluxes, salt crust characteristics, groundwater and climate at the Salar de Atacama, a 3000 km 2 playa in northern Chile containing a uniquely broad range of salt crust types. Land surface energy budget measurements were taken at eight representative sites on this playa during winter (August 2001) and summer (January 2002) seasons. Measured values of net all-wave radiation were highest at vegetated and rough halite crust sites and lowest over smooth, highly reflective salt crusts. Over most of the Salar de Atacama, net radiation was dissipated by means of soil and sensible heat fluxes. Dry salt crusts tended to heat and cool very quickly, whereas soil heating and cooling occurred more gradually at wetter vegetated sites. Sensible heating was strongly linked to wind patterns, with highest sensible heat fluxes occurring on summer days with strong afternoon winds. Very little energy available at the land surface was used to evaporate water. Eddy covariance measurements could only constrain evaporation rates to within 0.1 mm d −1, and some measured evaporation rates were less than this margin of uncertainty. Evaporation rates ranged from 0.1 to 1.1 mm d −1 in smooth salt crusts around the margin of the salar and from 0.4 to 2.8 mm d −1 in vegetated areas. No evaporation was detected from the rugged halite salt crust that covers the interior of the salar, though the depth to groundwater is less than 1 m in this area. These crusts therefore represent a previously unrecorded end member condition in which the salt crusts form a practically impermeable barrier to evaporation. 相似文献
2.
Bacterial abundances and activity, estimated by 4′,6-diamidino-2-phenylindole staining (DAPI) and the reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl tetrazolium chloride (INT), were investigated in two oligotrophic artificial groundwater lakes and the surrounding aquifers. To evaluate the effect of lake water on groundwater downstream, samples were taken from wells at different distances from the lakes, and the total number of bacteria and the number of active bacteria in these samples were compared with samples collected upstream. In addition, sterilized sandy sediments were exposed in groundwater wells to measure the number and activity of bacteria attached to particles. At one of the study sites, where the lake sediments were disturbed by dredging, total bacterial abundance and the number of respiring bacteria in the groundwater aquifer was clearly influenced by the lake water. The average bacterial abundances decreased from 2.6 ± 1.9 × 10 5 cells ml −1 in the well closest to the lake (S2) to 2.9 ± 3.8 × 10 4 cells ml −1 in the most distant one (S4), which was equivalent to cell numbers in the upstream well. The number of respiring bacteria showed a similar tendency with 1.3 ± 2.7 × 10 4 active cells ml −1 in S2 and 1.9 ± 1.5 × 10 3 active cells ml −1 in S4. At the second study site, which was not influenced by dredging, bacteria in the downstream wells seemed not to be affected by the lake water. The number and activity of bacteria, which colonized exposed sediments, were not significantly different in the upstream and downstream wells, indicating a minor influence of lake water on this habitat. Our results suggest that gravel-pit lakes may influence the free living bacterial assemblages in nearshore groundwater systems, but do not visibly affect numbers and activity of bacteria attached to the surface of aquifer sediments. 相似文献
3.
In the first part of this paper, the impact of forestry, agriculture and urban activities on the quality of surface water is analysed. Daily data from 15 forest and agricultural experimental catchments of the Institute of Hydrology, Slovak Academy of Sciences are used. It is shown, that the nitrate concentrations in surface water have decreased in Slovakia since 1989 as a result of decreased use of inorganic nitrogen fertilisers (lower intensity of agricultural production in Slovakia owing to recent economic changes). The annual nitrate specific load varies from 5.90 to 110 kg ha −1 year −1, the annual sulphate load varied from 29.16 to 509.60 kg ha −1 year −1 and the annual phosphate load varied from 0.0098 to 0.0224 kg ha −1 year −1 during 1990–1992. In the second part, a two-step method of three-component hydrograph separation of rain-, soil- and groundwater is proposed. The method is used in the Manelo-Gribov microbasin (O.95 km2) in Eastern Slovakia. The annual contribution of surface runoff in total runoff volume was 57.5%, the contribution of interflow runoff was 21.1%, and the contribution of groundwater was 21.4%, during the period from 1 August to 31 July 1992. A deterministic regression model for predicting daily nitrate concentrations from values of stream daily discharge and flow component data was developed. A set of 1421 modelled NO3−1 data was compared with the set of measured data. 相似文献
4.
Paleocene volcanic rocks in West Greenland and Baffin Island were among the first products of the Iceland mantle plume, forming part of a larger igneous province that is now submerged beneath the northern Labrador Sea. A 40Ar/ 39Ar dating study shows that volcanism commenced in West Greenland between 60.9 and 61.3 Ma and that 80% of the Paleocene lava pile was erupted in 1 million years or less (weighted mean age of 60.5±0.4 Ma). Minimum estimates of magma production rates (1.3×10 −4 km 3 year −1 km −1) are similar to the present Iceland rift, except for the uppermost part of the Paleocene volcanic succession where the rate decreases to <0.7×10 −4 km 3 year −1 km −1 (rift). The timing of onset of volcanism in West Greenland coincides with the opening of the northern Labrador Sea and is also strikingly similar to the age of the oldest Tertiary volcanic rocks from offshore SE Greenland and the British–Irish province. This is interpreted as manifesting the impact and rapid (>1 m/year) lateral spreading of the Iceland plume head at the base of the Greenland lithosphere at 62 Ma. We suggest that the arrival, or at least a major increase in the flux, of the Iceland mantle plume beneath Greenland was a contributing factor in the initiation of seafloor spreading in the northern Labrador Sea. Our study has also revealed a previously unrecognised Early Eocene volcanic episode in West Greenland. This magmatism may be related to movement on the transform Ungava Fault System which transferred drifting from the Labrador Sea to Baffin Bay. A regional change in plate kinematics at 55 Ma, associated with the opening of the North Atlantic, would have caused net extension along parts of this fault. This would have resulted in decompression and partial melting of the underlying asthenosphere. The source of the melts for the Eocene magmatism may have been remnants of still anomalously hot Iceland plume mantle which were left stranded beneath the West Greenland lithosphere in the Early Paleocene. 相似文献
5.
In 1989, in a hydrological research programme within a deacidification project in the Gårdsjön area in southwest Sweden, flow paths and residence times of soil water and groundwater in microcatchments were examined to support the interpretation of the hydrochemical changes. Saturated hydraulic conductivity and soil water retention were analysed on more than 100 cylinder samples. The catchments have shallow sandy-silty till soil with a mean depth in the main catchment of 43 cm. Porosity of the mineral soil in the main catchment was high and ranged from 38 to 85%. The samples from the B-horizon had generally higher porosity. Porosity and the content of organic matter were correlated. The soil water retention was relatively high at all tensions, likely owing to the high content of organic matter. Dissolved organic substances were most probably transported from the shallow soil on the steep sides of the catchment down to the valley where it precipitated. The high porosities could be a consequence of long-term weathering, provided that the organic substances present have increased the leaching of the weathering products. Measured values of saturated hydraulic conductivity were close to log-normally distributed with a mean for all samples of 3 × 10 −5 m s −1. There was a significant increase in conductivity toward the ground surface with the mean conductivity of the samples in the uppermost 10 cm of the mineral soil of 4 × 10 −5 m s −1, which was about 13 times higher than the conductivity of 3 × 10 −6 m s −1 at 1 m depth. From the relationship between runoff at the catchment outlet and groundwater levels, the conductivity was estimated to be 15–200 times higher in the upper soil layer than in the deeper ones. In one profile, 44–64% of the yearly lateral flow was estimated to occur above 30 cm depth. The conductivity was correlated with the content of drainable water, which indicated the importance of the largest pores for the saturated hydraulic conductivity. 相似文献
6.
Water-budget components and the vertical conductance were determined for Lowry (Sand Hill) Lake in north-central Florida, USA. In this type of lake, which interacts with both the surface-water and groundwater systems, the inflow components are precipitation, surface-water inflow, groundwater inflow, and direct runoff (i.e. overland flow), and the outflow components are evaporation, groundwater outflow, and surface-water outflow. In a lake and groundwater system that is typical of many karst lakes in Florida, a large part of the groundwater outflow occurs by means of vertical leakage through an underlying confining unit to a deeper, highly transmissive aquifer called the upper Floridan aquifer. The water-budget component that represents vertical leakage to the upper Floridan aquifer was calculated as a residual using the water-budget equation. For the 13 month period from August 1994 to August 1995, relative to the surface area of the lake, rainfall at Lowry Lake was 1.55 m yr −1, surficial aquifer inflow was 0.79 m yr −1, surface-water inflow was 1.92 m yr −1, and direct runoff was 0.01 m yr −1. Lake evaporation was 1.11 m yr −1, and surface-water outflow was 1.61 m yr −1. The lake stage increased 0.07 m yr −1, and the vertical leakage to the upper Floridan aquifer was 1.48 m yr −1. Surficial aquifer outflow from the lake was negligible. At Lowry Lake, vertical leakage is a major component of the water budget, comprising about 35% of the outflow during the study period. The vertical conductance ( KV/ b), a coefficient that represents the average of the vertical conductances of the hydrogeologic units between the bottom of a lake and the top of the upper Floridan aquifer, was determined to be 2.51 × 10 −4 day −1 for Lowry Lake. 相似文献
7.
To examine nitrate persistence, detailed geochemical profiling, using core-squeezed water and piezometer samples, was carried out at five sites in southern Ontario where groundwater is moving downward in silt-rich aquitard sediments at rates of 16 to more than 20 cm year −1. Elevated levels of NO 3−-N (5–50 mg 1 −1) that occur in the shallow groundwater as a result of agricultural activity, were found to be consistently attenuated, generally to very low levels (< 0.05 mg 1 −1-N), at the ‘redoxcline’, the horizon marking the boundary between the surficial weathered (brown) sediments and the underlying unweathered (grey) sediments. Tritium dating suggests that groundwater at the redoxcline depths (3–5 m) was recharged between 1970 and 1980, thus the N03 depletion appears to result from biodegradation reactions since no major landuse changes have occurred during this period. The close association of the nitrate depletion zones with the redoxcline, where, in particular, sediment sulphur contents increase abruptly, and where also porewater SO 42− levels increase, suggests that the dominant attenuation reaction is autotrophic denitrification using reduced sulphur compounds present in the unweathered sediment as the electron donor. Mass balance calculations suggest that the increase in the downward rate of migration of the redoxcline, owing to added sulphur consumption from NO 3− contamination, is only about 1 mm year −1 at these sites. Review of the literature indicates that most silt- and clay-rich sediments have S contents in the same range, or higher, than those investigated here, thus, in most cases where aquifers are overlain by several metres or more of unweathered confining sediments, it is likely that a high degree of protection is afforded from surficial NO 3− contamination. 相似文献
8.
Nine years of bulk precipitation chemistry data for a mountainous site in southern France are presented. The mean rainwater is of moderate acidity (pH 4.63, alkalinity −4 μEql −1) even though there is high, non-marine, deposition of sulphur (near 20 kg ha −1 year −1). Based on the statistical characteristics of the data set, three major sources of elements are identified: long range pollution, Mediterranean sea salt aerosols and aeolian erosion dust, mainly from the Sahara. Most of the sulphur in the rainfall is present as neutral sulphate salts, owing to the latter being rich in alkaline minerals; this counteracts the strong acid input. 相似文献
9.
Analytical procedures in the determination of iodine-129 (half-life: 1.6×10 7 y) have been studied using accelerator mass spectrometry (AMS), with special references to the separation procedures of iodine from soil samples for the AMS measurement. Iodine was successfully volatilized from soil samples by pyrohydrolysis at 1000 °C and collected in a trap solution. Iodine was purified from the matrix by solvent extraction. Finally, it was precipitated as silver iodide to make a target for AMS. In order to obtain information on the 129I/ 127I ratio in a chemical blank (or iodine carrier), we have determined the ratios in several iodine reagents and found that the ratios fell in a narrow range around 1.7×10 −13. The detection limit for soil sample (1 g material) by the present method was about 0.01 mBq/kg or 4×10 −11 as the ratio of stable iodine ( 129I/ 127I ratio), i.e. these values were much better than that by neutron activation analysis (NAA) used in our previous studies. We have applied this method in the analysis of soil samples collected from different places in Japan. We could successfully determine 129I in soil samples with low 129I concentrations, which could not be detected by NAA. Sample size necessary for the soil analysis by AMS was only about 0.5 g or less, whereas about 100 g of the sample were required for NAA [Muramatsu, Y., Ohmomo, Y., 1986. Iodine-129 and iodine-127 in environmental samples collected from Tokaimura/ Ibaraki, Japan. Sci. Total Environ. 48, 33-43]. Using this method, new data were obtained for the 129I levels in 20 soil samples collected from background areas far from nuclear facilities, and the ranges were 1.4×10 −5−4.5×10 −3 Bq/kg as 129I concentrations and 3.9×10 −11−2.2×10 −8 as 129I/ 127I ratios. These values are useful in understanding the 129I levels in Japanese environments. Higher 129I concentrations were observed in forest soils than those in field and rice paddy soils should be related to the interception effect of atmospheric 129I due to tree canopies. Relatively high 129I/ 127I ratios found in rice paddy soils could be explained by their low stable iodine concentrations which were caused by the desorption of stable iodine from the rice paddies during the cultivation. 相似文献
10.
Water sampling during the 1993 IV Russian–US Joint Expedition to the Bering and Chukchi Seas (BERPAC) indicates that Pacific Ocean burdens of the long-lived radionuclide 129I are relatively low in the Pacific-influenced Arctic, particularly compared to high latitude waters influenced by the North Atlantic. These low concentrations occur despite the presence of potential submerged anthropogenic sources in the East Sea (Sea of Japan), and in the northwest Pacific Ocean, east of the Kamchatka Peninsula. The concentration of 129I entering the Arctic Ocean through Bering Strait, 0.7×10 8 atoms kg −1, is only slightly higher than observed in deep Pacific waters. Similar concentrations (0.44–0.76×10 8 atoms kg −1) measured in Long Strait indicate no significant transfer of 129I eastward into the Chukchi Sea in the Siberian Coastal Current from the Siberian marginal seas to the west. However, the concentrations reported here are more than an order of magnitude higher than the Bering Strait input concentration estimated (1.0×10 6 atoms kg −1) from bomb fallout mass balances, which supports other existing evidence for a significant atmospheric deposition term for this radionuclide in surface ocean waters. Near-bottom water samples collected in productive waters of the Bering and Chukchi Seas also suggest that sediment regeneration may locally elevate 129I concentrations, and impact its utility as a water mass tracer. As part of this study, two deep 129I profiles were also measured in the East Sea in 1993–1994. The near-surface concentration of 129I ranged from 0.12 to 0.31×10 8 atoms kg −1. The 129I concentration showed a steady decrease with depth, although because of active deep water ventilation, the entire 3000 m water column exceeded natural concentrations of the radionuclide. Atom ratios of 129I/ 137Cs in the East Sea also suggest an excess of 129I above bomb fallout estimates, also possibly resulting from atmospheric deposition ultimately originating from nuclear facilities. 相似文献
11.
The impact of domestic sewage effluent (SE) on the dynamics of phytoplankton assemblages from Bedford Basin was evaluated in the laboratory. Phytoplankton production and chlorophyll a increased proportionally with SE enrichment. Phytoplankton species composition also changed. The potentially harmful diatoms, Pseudonitzschia spp., present initially in small numbers (600 cells 1 −1) in Bedford Basin seawater, and became dominant (3–5×10 6 cells 1 −1) when the seawater was enriched with 0.5–5% untreated SE. With higher proportions of SE, other harmful species such as Fragilaria spp. and Euglena spp. became dominant (7−15×10 6 and 2.2×10 4 cells 1 −1, respectively). Treatment of SE with UV light or activated charcoal seems to favour growth of benign species, such as Chaetoceros socialis, Skeletonema costatum and Thalassiosira spp., but not harmful species such as Pseudonitzschia spp. Further research on UV treatment of domestic sewage is recommended. 相似文献
12.
Noble gases were extracted in steps from grain size fractions of microdiamonds ( < 100 μm) from the Kokchetav Massif, Northern Kazakhstan, by pyrolysis and combustion. The concentration of 4He in the diamonds proper (liberated by combustion) shows a 1/ r dependence on grain size. For grain diameters > 15 μm the concentration also decreases with the combustion step. Both results are clear evidence that 4He has been implanted into the diamonds from -decaying elements in the surrounding matrix. The saturation concentration of 4He(5.6 × 10 −4 cm 3 STP/g) is among the very highest observed in any terrestrial diamonds. Fission xenon from the spontaneous fission of 238U accompanies the radiogenic 4He; the 136Xe f/ 4He ratio of (2.5 ± 0.3) × 10 −9 agrees well with the production ratio of 2.3 × 10 −9 expected in a reservoir where Th/U 3.3. Radiogenic 40Ar is predominantly ( > 90%) set free upon combustion; it also resides in the diamonds and appears to have been incorporated into the diamonds upon their formation. 3He, on the other hand is mainly released during pyrolysis and hence is apparently carried by ‘contaminants’. The concentration in the diamonds proper is of the order of 4 × 10−12 cm3 STP/g, with a 3He/4He ratio of 1 × 10−8. Excess 21Ne, similarly, appears to be present in contaminants as well as in diamonds proper. These two nuclides in the contaminants must have a nucleogenic origin, but it is difficult to explain their high concentrations. 相似文献
13.
The formation and development of a salt plume (salinity up to 800 mg Cl 1 −1) in the inner part of the Coastal Plain aquifer of Israel is analyzed. Massive groundwater exploitation during the 1950s caused a large drop in the water level and formation of a hydrologic depression in the Be'er Toviyya-Kefar Warburg area. The depression reached a maximal depth during the late 1960s; thereafter a reduction in the rate of pumpage led to restoration of water levels and shallowing of the depression, until its complete disappearance towards the end of the 1980s. A spot of high salinity first appeared in 1956, following a deep drawdown in the water levels. This saline plume has been continuously expanding with increasing salinity concentrations (200–800 mg Cl 1 −1) in its center. The average rate of radial expansion was about 50 m year −1. The expansion and salinization did not cease as the depression disappeared. Rather, equalization of water levels in wells situated within the plume area with those of situated along its margins resulted in the salinization of the latter within a period of 1 year. Mass balances for water and chloride contents were made for the period 1967–1990. Taking into consideration the storage change, pumpage, natural replenishment and artificial recharge, the lateral inflow to the depression is estimated as 60 × 106 m3. Upon addition of the chloride balance, and taking into consideration the chloride concentrations of the surrounding fresh water and the apparent possible end-member of the saline source (based on geochemical considerations), the saline inflow is estimated as (40–60) × 106 m3. These estimates indicate that a large amount of saline water penetrated into the aquifer, of about half of the natural replenishment of the study area, with an estimated salinity of 1900–2700 mg Cl 1−1. It is suggested that the salt plume was formed as a result of a drop in water level combined with a flow of underlying saline water bodies from deeper strata. The chemical composition of the groundwater points to the existence of two saline water bodies of Ca-chloride composition and a marine Br/Cl ratio: (1) saline water with low Na/Cl (0.6), So4/Cl, and B/Cl ratio; (2) saline water with higher Na/Cl (> 0.6), So4/Cl, and B/Cl ratios. These chemical compositions resemble Ca-chloride saline waters found in other locations in the Coastal Plain aquifer and in underlying formations. The saline water bodies may occur in either pockets at the bottom of the aquifer or lumachelle and sandstone layers of high hydraulic conductivity in underlying sediments. 相似文献
14.
Isotope and hydrochemical data of the thermal water system in Cieplice
laskie Zdrój (Spa) indicate the existence of two subsystems that greatly differ in volume and which meet at the fault zones of a granitic horst, where they discharge at an altitude of about 340m. One of the subsystems is very small (about 4 × 10 3 m 3) as indicated by the tritium age of the order of 10 years and a low outflow rate. Its recharge area found from the δ 18O and δD values, is about 200m above the springs, most probably on the slopes of the foothills of the Karkonosze Mountains south-southwest of the spa. The large subsystem contains water which is free of tritium and whose 14C content is from 1 to 8 pmc with δ 13C = −8.0 to −9.2‰. The isotopic composition of this water reflects either the climatic effect (low-altitude recharge during a cooler pre-Holocene climate) or the altitude effect (recharge in the early Holocene period at about 1000m at the heights of the Karkonosze assuming that the 14C concentration is strongly reduced by exchange with calcite in veins). For the former hypothesis, the recharge area of this water is probably either at the foot of the southeastern slopes of the Kaczawa Mountains or/and at the foot of the Rudawy Janowickie Mountains, to the east of Cieplice. The noble gas temperatures are more consistent with the pre-Holocene recharge. Similarly, the 4He excess and 40Ar/ 36Ar ratio support the hypothesis of a pre-Holecene age. The constant 3He/ 4He ratio of 26 × 10 −8 for highly different helium contents indicates crustal origin of helium. For the pre-Holocene age of water its volume is calculated at >- 10 9m 3 (stagnant water in micropores and mobile water in fractures) and the hydraulic conductivity of the host granite massif is estimated at about 7 × 10 −8 ms −1. Two outflows from this subsystem have different and variable fractions of a modern water component (bomb age), most probably originating from the bank infiltration of a nearby stream. 相似文献
15.
This study aimed to determine whether the δ 13C levels in the foliage and twigs of four Eucalyptus grandis clones were related to their water use efficiency (WUE). This relationship has previously been demonstrated in a number of herbaceous species but not in mature trees. The study involved accurate measurements of tree trunk growth and water use over a period of 4 months, with subsequent isotopic analysis of mature foliage from the north and south side of the canopy, and young leaves from the top of the canopy. The water use efficiencies were found to vary from 5.97 × 10−3 to 12.3 × 10−3 m3 m−3. Significant differences were observed between clonal-mean water use efficiencies averaged over six sampling periods. The average δ13C of the mature and young foliage was found to be significantly correlated with WUE. However, the correlation was weak, suggesting that the relationship between δ13C and WUE is more complex in trees than suggested in the literature on crop plants. It is suggested that differences between sample trees in carbon allocation and leaf-to-air vapour pressure deficits may account for the poor correlation between δ13C and WUE in the four E. grandis clones studied. 相似文献
16.
We have developed techniques to determine 238U, 234U and 232Th concentrations in seawater by isotope dilution mass spectrometry. U measurements are made using a 233U 236U double spike to correct for instrumental fractionation. Measurements on uranium standards demonstrate that 234U/ 238U ratios can be measured accurately and reproducibly. 234U/ 238U can be measured routinely to ± 5‰ (2σ) for a sample of 5 × 10 9 atoms of 234U (3 × 10 −8 g of total U, 10 ml of seawater). Data acquisition time is 1 hour. The small sample size, high precision and short data acquisition time are superior to-counting techniques. 238U is measured to ± 2‰ (2σ) for a sample of 8 × 10 12 atoms of 238U ( 3 × 10 −9 g of U, 1 ml of seawater). 232Th is measured to ± 20‰ with 3 × 10 11232Th atoms (10 −10 g 232Th, 1 1 of seawater). This small sample size will greatly facilitate investigation of the 232Th concentration in the oceans. Using these techniques, we have measured 238U, 234U and 232Th in vertical profiles of unfiltered, acidified seawater from the Atlantic and 238U and 234U in vertical profiles from the Pacific. Determinations of 234U/ 238U at depths ranging from 0 to 4900 m in the Atlantic (7°44′N, 40°43′W) and the Pacific (14°41′N, 160°01′W) Oceans are the same within experimental error (± 5‰,2σ). The average of these 234U/ 238U measurements is 144 ± 2‰ (2σ) higher than the equilibrium ratio of 5.472 × 10 −5. U concentrations, normalized to 35‰ salinity, range from 3.162 to 3.281 ng/g, a range of 3.8%. The average concentration of the Pacific samples (31°4′N, 159°1′W) is 1% higher than that of the Atlantic (7°44′N, 40°43′W and 31°49′N, 64°6′W). 232Th concentrations from an Atlantic profile range from 0.092 to 0.145 pg/g. The observed constancy of the 234U/ 238U ratio is consistent with the predicted range of 234U/ 238U using a simple two-☐ model and the residence time of deep water in the ocean determined from 14C. The variation in salinity-normalized U concentrations suggests that U may be much more reactive in the marine environment than previously thought. 相似文献
17.
The activity ratios of Pu and radiocesium isotopes have been used to delineate the major sources (such as global and close-in (debris) fallout, nuclear fuel reprocessing and fabrication plant effluents) in the environment. We have measured 238Pu, 239,240Pu, 137Cs, and excess 210Pb concentrations in 107 surficial sediments as well as in 5 sediment cores collected in the summer months of 1993 and 1994 from the Ob and Yenisey Rivers (Russia) and the Kara sea. A comparison of the sediment core inventories of 239,240Pu and 137Cs, along with the 238Pu/ 239,240Pu activity ratios, with those expected from global fallout allows us to estimate the relative amounts, if any, of reactor-derived 238Pu and 239,240Pu from the dumped reactor sites in the study area. In surficial sediment samples collected in 1993 and 1994, the 239,240Pu concentrations varied between 4.2 and 856 mBq kg−1, with a mean of 239 mBq kg−1. In samples with a measurable 238Pu, the 238Pu/239,240Pu activity ratios varied between 0.010 and 0.069, with an average value of 0.035 ± 0.014. This range can be compared to the average 238Pu/239,240Pu activity ratio of 0.030 for the year 1993 from nuclear weapons testing and SNAP fallout obtained from soil studies, indicating very little (≤ 5%) additional sources of 238Pu to the sediments in the study area. The inventories of Pu in the 5 sediment cores from the study area varied between 2.67 ± 0.67 and 24.5 ± 2.2 Bq m−2 with a mean value of 8.83 Bq m−2. The 137Cs concentrations in the upper 3 cm of the sediments varied between below detection limit to 71.4 Bq kg−1, with a mean of 14.9 Bq kg−1. The 137Cs inventories in the 5 sediment cores varied between 156.7 ± 28.3 and 1600 ± 153.3 Bq m−2, with a mean value of 583.3 Bq m−2. The mean ratio of inventories of Pu to that of 137Cs, 0.015, is comparable to the values in other places in the Arctic region. There is a significant correlation between total organic carbon and concentrations of 137Cs, 239,240Pu and 210Pb, suggesting that organic matter-enriched fine particles are a likely carrier phase for these nuclides. The ratio of 137Cs/239,240Pu also suggests that most of these nuclides are derived from global fallout. 相似文献
18.
In eastern England the Chalk aquifer is covered by extensive Pleistocene deposits which influence the hydraulic conditions and hydrochemical nature of the underlying aquifer. In this study, the results of geophysical borehole logging of groundwater temperature and electrical conductivity and depth sampling for major ion concentrations and stable isotope compositions (δ 18O and δ 2H) are interpreted to reveal the extent and nature of the effective Chalk aquifer of north Norfolk. It is found that the Chalk aquifer can be divided into an upper region of fresh groundwater, with a Cl concentration of typically less than 100 mg l −1, and a lower region of increasingly saline water. The transition between the two regions is approximately 50 m below sea-level, and results in an effective aquifer thickness of 50–60 m in the west of the area, but less than 25 m where the Eocene London Clay boundary is met in the east of the area. Hydrochemical variations in the effective aquifer are related to different hydraulic conditions developed in the Chalk. Where the Chalk is confined by low-permeability Chalky Boulder Clay, isotopically depleted groundwater (δ 18O less than −7.5‰) is present, in contrast to those areas of unconfined Chalk where glacial deposits are thin or absent (δ 18O about −7.0‰). The isotopically depleted groundwater is evidence for groundwater recharge during the late Pleistocene under conditions when mean surface air temperatures are estimated to have been 4.5°C cooler than at the present day, and suggests long groundwater residence times in the confined aquifer. Elevated molar Mg:Ca ratios of more than 0.2 resulting from progressive rock-water interaction in the confined aquifer also indicate long residence times. A conceptual hydrochemical model for the present situation proposes that isotopically depleted groundwater, occupying areas where confined groundwater dates from the late Pleistocene, is being slowly modified by both diffusion and downward infiltration of modem meteoric water and diffusive mixing from below with an old saline water body. 相似文献
19.
Tributyltin (TBT) concentrations in waters of Poole Harbour ranged between 2–139 ng l −1 (as Sn) and increased to 234–646 ng l −1 within marinas. Seasonal trends in contamination coincided with boat usage patterns and peaked during summer months. A combination of poor tidal flushing and removal of TBT to particulates restricts high levels of contamination to areas closest to marinas and moorings; TBT concentrations in benthic sediments decreased from 0.52 μg g −1 near such sites to 0.02 μg g −1 at the harbour mouth. Organotin accumulations in several benthic invertebrates including polychaetes (Nereis diversicolor), snails (Littorina littorea) and clams (Scrobicularia plana, Mya arenaria) reflect the distribution of contamination in the environment, though concentration factors (relative to water) vary considerably between species and were highest in sediment dwelling clams, notably Mya (1.3×10 5). Compared to organotins, biological availability of inorganic tin is low. Levels of TBT in parts of Poole Harbour exceed Environmental Quality Targets designed to protect marine life and may be responsible for poor recruitment, particularly in bivalves, at heavily contaminated sites. 相似文献
20.
Gas is extracted from large (6–31 kg) Antarctic ice samples to obtain sufficient CO 2 for 14C measurements with small low-level proportional counters. The 14C ages of Byrd core ice are in accord with glaciological estimates ranging from (2.2 −1.1+1.4)×10 3 yr at 271 m depth to more than 8 × 10 3 yr at 1071 m depth. The CO 2 abundances in gas extracted from Byrd core ice range from 0.0216 to 0.051%, with below present-day atmosphere CO 2 abundances for ice from 1068 and 1469 m depths. The CO 2 abundance in gas from Allan Hills surface ice samples ranges between four and six times the atmospheric value and the CO 2 had a specific activity three times that of contemporary carbon. A possible explanation for the anomalously high specific activity is surface melting with the incorporation into CO 2 of 14C produced by cosmic ray spallation of oxygen in ice. The CO 2 abundance in gas extracted from subsurface Allan Hills ice ranged from 0.030 to 0.065%, and the specific activities are below contemporary carbon, indicating ages greater than 5×10 3 yr. The 18O/ 16O ratio of oxygen in the trapped gas is the same as that of atmospheric oxygen and differs markedly from the 18O/ 16O ratio in the ice. The O 2, N 2, and Ar abundances and isotopic compositions are similar to those in contemporary air, except for positive 15N/ 14N ratios in a few samples. 相似文献
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