首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
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   


2.
S. V. Panno  W. R. Kelly   《Journal of Hydrology》2004,290(3-4):229-242
This investigation was designed to estimate the mass loading of nitrate (NO3−) and herbicides in spring water discharging from groundwater basins in an agriculturally dominated, mantled karst terrain. The loading was normalized to land use and NO3− and herbicide losses were compared to estimated losses in other agricultural areas of the Midwestern USA. Our study area consisted of two large karst springs that drain two adjoining groundwater basins (total area of 37.7 km2) in southwestern Illinois' sinkhole plain, USA. The springs and stream that they form were monitored for almost 2 years. Nitrate–nitrogen (NO3–N) concentrations at three monitoring sites were almost always above the background concentration (1.9 mg/l). NO3–N concentrations at the two springs ranged from 1.08 to 6.08 with a median concentration of 3.61 mg/l. Atrazine and alachlor concentrations ranged from <0.01 to 34 μg/l and <0.01 to 0.98 μg/l, respectively, with median concentrations of 0.48 and 0.12 μg/l, respectively. Approximately 100,000 kg/yr of NO3–N, 39 kg/yr of atrazine, and 2.8 kg/yr of alachlor were discharged from the two springs. Slightly more than half of the discharged NO3− came from background sources and most of the remainder probably came from fertilizer. This represents a 21–31% loss of fertilizer N from the groundwater basins. The pesticide losses were 3.8–5.8% of the applied atrazine, and 0.05–0.08% of the applied alachlor. The loss of atrazine adsorbed to the suspended solid fraction was about 2 kg/yr, only about 5% of the total mass of atrazine discharged from the springs.  相似文献   

3.
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   

4.
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   


5.
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 km3 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 km3 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   

6.
Most lead brought to the Mediterranean Sea has an anthropogenic origin and is mainly transported through the atmosphere. Atmospheric Pb was continuously collected at Cap Ferrat in 1986 and 1987. From this study, the estimation of the anthropogenic Pb flux on the whole Western Mediterranean was, averaged on 1986 and 1987 data, 4080 t. Assuming that the atmospheric anthropogenic Pb input varied in this course of time similarly to the consumption of Pb added to gasolines in France, the mean annual flux could be calculated: 3.95 kg km−2 yr−1, that is an annual input of 3360 t yr−1. Reaching the sea, this metal seems to become rapidly bound to phytoplankton. Grazing by zooplankton leads to the production of faecal pellets which frequently contain rather high metal concentrations. The sinking rate of pellets of various zooplankton species is high; within a few days pellets may reach deep-sea sediments. After deposition, Pb is released from this organic-rich material during early diagenesis. In most cases, it, therefore, returns to the overlaying water body by ascending diffusion. But, in a deep-sea area of approximately 80 000 km2 where Mn oxide precipitation occurs in surficial sediments, Pb seems to remain stored by coprecipitation processes. By considering the lead stored in ‘excess’ in the surficial sediment of the deep-sea area, we estimate that a mean annual anthropogenic Pb amount ranging from 800 up to 1080 t was stored every year from 1950. On the same area, taking into account the Pb loss at the straits, the ‘direct’ atmospheric input to the sea bottom is, on average, 184 t yr−1. The remaining part, that is (800–1080)−184=(616–896) t yr−1, corresponds to an additional ‘indirect’ Pb flux in water due to Pb released from sediments of the surrounding areas where it does not remain stored.  相似文献   

7.
Concentrations of the sum of 15 PAHs in 22 surficial sediment samples from the western Irish Sea ranged from below 100 ng g−1 in sandy sediments to a maximum of 1422 ng g−1 in the centre of the mud basin. The concentrations are typical of coastal shelf sediments, but greater than those observed for aquatic sediments remote from known anthropogenic sources. Organic C and the % sediment <15 μm were positively correlated with ΣPAH. ΣPAH was normalised to organic C and particle size (i.e. expressed as ΣPAH/Corg and ΣPAH/%<15 μm) and significant relationships were still observed with organic C and %<15 μm. The results are discussed in the context of using organic C to normalise concentrations of PAHs to assess contamination levels in sediments.  相似文献   

8.
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 cm3 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 136Xef/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   


9.
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   

10.
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 × 105 cells ml−1 in the well closest to the lake (S2) to 2.9 ± 3.8 × 104 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 × 104 active cells ml−1 in S2 and 1.9 ± 1.5 × 103 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   

11.
REE diffusion in calcite   总被引：6，自引：0，他引：6  
Chemical diffusion of four rare-earth elements (La, Nd, Dy and Yb) has been measured in natural calcite under anhydrous conditions, using rare-earth carbonate powders as the source of diffusants. Experiments were run in sealed silica capsules along with finely ground calcite to ensure stability of the single-crystal samples during diffusion anneals. Rutherford backscattering spectroscopy (RBS) was used to measure diffusion profiles. The following Arrhenius relations were obtained over the temperature range 600–850°C: DLa =2.6×10−14 exp(−147±14 kJ mol−1/RT) m2 s−1, DNd =2.4×10−14 exp(−150±13 kJ mol−1/RT) m2 s−1, DDy =2.9×10−14 exp(−145±25 kJ mol−1/RT) m2 s−1, DYb =3.9×10−12 exp(−186±23 kJ mol−1/RT) m2 s−1. In contrast to previous findings for refractory silicates (e.g. zircon), differences in transport rates among the REE are not pronounced over the range of temperature conditions investigated in this study. Diffusion of the REE is significantly slower than diffusion of the divalent cations Sr and Pb and slower than transport of Ca and C at temperatures above 650°C. Fine-scale zoning and isotopic and REE chemical signatures may be retained in calcites under many conditions if diffusion is the dominant process affecting alteration.  相似文献   

12.
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 (3–5×106 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 (7−15×106 and 2.2×104 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   

13.
This paper addresses the distribution, origin and controls upon nitrate in a 30-km2 area of the Interior Great Plains Region of southern Alberta, Canada. High concentrations of nitrate (> 100 mg l−1 NO−3-N) occurred in several isolated enclaves below the water table in brown weathered till. Nitrate concentrations of over 300 mg l−1-N were encountered in groundwater samples collected from these enclaves. Low nitrate concentrations (< 1.1 mg l−1 NO−3-N) were also encountered in the weathered till upgradient and downgradient of the nitrate enclaves. Groundwater samples collected from the underlying grey nonweathered till and bedrock had NO−3-N concentrations of < 1.1 mg l−1.

Through the application of geochemical (NO−3-N and NH+4-N) studies, environmental isotope studies (tritium), microbial analyses (nitrifiers) and laboratory experiments, it was shown that the high nitrates found in the weathered till are the result of the oxidation of ammonium present within the tills. It is postulated that this oxidation occurred during the Holocene epoch when water tables were much lower than present-day levels (5–18 m, and 2 m below ground, respectively).

Through the use of Eh measurements, the enumeration of denitrifying bacteria and laboratory experiments, the potential for denitrification was shown to exist below the present-day water table in the weathered till as well as in the nonweathered till and bedrock. Isotopic data showed that less denitrification may be occurring within the nitrate enclaves than in adjacent downgradient areas.  相似文献   


14.
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   

15.
This research (1) characterized the effects of sublethal cupric ion activities on the grazing behavior of two estuarine copepods (Acartia tonsa, Acartia hudsonica) and one nearshore, neritic copepod (Temora longicornis) and (2) compared the sensitivity of short-term sublethal behavioral assays with that of longer-term acute toxicity tests. A nitrilotriacetate-trace-metal-ion buffer system at 27‰. S was used to quantify and control the free cupric ion activity. Acute toxicity tests were used to determine the mortality of A. tonsa and T. longicornis over 72 h within the approximate cupric ion activity range of 10−13 to 10−9.5 M. 24 h survival was not affected within the approximate cupric ion activity range of 10−13 to 10−9.7 M, the range used for subsequent grazing activity experiments after 24 h exposure to Cu. Grazing activity was significantly diminished at cupric ion activities of ≈ 10−10 M for A. tonsa and T. longicornis, and at ≈ 10−11 M for A. hudsonica. A hormetic pattern of response in feeding activity was observed with A. tonsa and T. longicornis. Grazing activity was found to be a sensitive measure of sublethal Cu stress compared with the acute toxicity tests. Grazing activity was affected at environmentally relevant cupric ion activities.  相似文献   

16.
238U, 232Th, 230Th and 226Ra abundances have been measured in six samples of recent Hawaiian basalt by high precision mass spectrometry, in an attempt to compare the melting process in plumes and at spreading ridges. The data reveal a very small range in (230Th/238U) activity ratio up to a maximum value of 1.02 ± 0.01, and (226Ra/230Th) activity ratios which lie between 1.10 ± 0.015 and 1.19 ± 0.02. UTh and RaTh abundances are linearly correlated demonstrating that the disequilibria predate crystallisation and differentiation. Using recently published estimates for the bulk partition coefficients of U and Th, the results are consistent with melting rates > 10−3 kg m−3 a−1 at porosities < 10−3 for dynamic fractional melting in the garnet stability field.  相似文献   

17.
In 1995–1998, Han 11 km terrestrial surge of Kuannersuit Glacier, an outlet glacier of the largest ice cap on Disko Island, West Greenland, affected the catchment dramatically. In order to estimate solute fluxes and provenances, bulk meltwaters were sampled at the main subglacial outlet during the initial part of the quiescent phase. The hydrochemistry is significantly influenced by a subglacial basaltic weathering regime with absence of carbonate minerals. The results show that marine and aerosol derived solutes have minimal contribution to the total ion content, whereas sequestration of atmospheric CO2 associated with carbonation of Ca-rich feldspar and reactive volcanic glass is more dominant than previously reported from glacierized catchments. Application of a sampling strategy dividing water samples into four groups to determine the content of dissolved HCO3− and CO32− shows that the cationic equivalent weathering rate range is 683–860 Σmeq+ m−2 a−1 and solute flux ranges between 76 and 98 t km−2 a−1. The crustal denudation rate is estimated to 26 t km−2 a−1, and the transient CO2 drawdown amounts to 8500–13700 kg C km−2 a−1.  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 (δ18O and δ2H) 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 (δ18O less than −7.5‰) is present, in contrast to those areas of unconfined Chalk where glacial deposits are thin or absent (δ18O 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.
A case study on fuel oil contamination in a mangrove swamp in Hong Kong   总被引：5，自引：0，他引：5  
Tam NF  Wong TW  Wong YS 《Marine pollution bulletin》2005,51(8-12):1092-1100
Mangroves commonly found along tropical and subtropical coastlines are susceptible to oil pollution. In December 2000, around 500 1 m tall Kandelia candel saplings at the age of 3–5 years old located at the foreshore region of Sheung Pak Nai swamp, Hong Kong SAR, were found to be damaged by oil pollution. More than 80% of the saplings were either dead or washed away and leaving less than 5% healthy saplings with dense green leaves. Elevated concentrations of light n-alkanes (ranging from n-C14 to n-C20), pristane and phytane were recorded in surface sediments collected in December 2000. The ratio between light and total n-alkanes was 0.4. The total petroleum hydrocarbons (60–80 μg g−1 TPH) and unresolved complex mixtures (60–70 μg g−1 UCM) were higher than the background values of other mangrove sediments in Hong Kong, which were 40 and 20 μg g−1, respectively. In certain root zone sediments, TPH concentrations were above 1000 μg g−1. These results suggest that surface sediments in Sheung Pak Nai were contaminated by petroleum oil, most likely by illegal discharge of fuel oil which occurred between 1998 and 2002. One year later, in December 2001, unhealthy saplings had recovered and re-grown. The concentrations of TPH and UCM in sediments declined to around 40 μg g−1, pristane and phytane dropped by 80%, and the ratio of light to total n-alkanes was 0.15, suggesting that residual oil in sediments was weathered leading to a remarkable recovery of the unhealthy saplings.  相似文献   

20.
We have developed techniques to determine238U,234U and232Th concentrations in seawater by isotope dilution mass spectrometry. U measurements are made using a233U236U double spike to correct for instrumental fractionation. Measurements on uranium standards demonstrate that234U/238U ratios can be measured accurately and reproducibly.234U/238U can be measured routinely to ± 5‰ (2σ) for a sample of 5 × 109 atoms of234U (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 × 1012 atoms of238U ( 3 × 10−9 g of U, 1 ml of seawater).232Th is measured to ± 20‰ with 3 × 1011232Th atoms (10−10 g232Th, 1 1 of seawater). This small sample size will greatly facilitate investigation of the232Th concentration in the oceans. Using these techniques, we have measured238U,234U and232Th in vertical profiles of unfiltered, acidified seawater from the Atlantic and238U and234U in vertical profiles from the Pacific. Determinations of234U/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 these234U/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 the234U/238U ratio is consistent with the predicted range of234U/238U using a simple two-☐ model and the residence time of deep water in the ocean determined from14C. 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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号