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1.
Sediment accumulation rate studies utilizing excess 210Pb and 137Cs were conducted as part of recent investigations of biogeochemical cycling at a single site in Cape Lookout Bight, a rapidly changing coastal basin on the Outer Banks of North Carolina (U.S.A.). Cores three meters in length reveal a depositional history for the bight interior characterized by a gradual transition in texture from coarse-grained to fine-grained material over the period 1946–1979. This transition is controlled by progressive enclosure of the bight by an active northerly migrating recurved spit. The textural gradation is periodically interrupted by layers of well-sorted sand associated with major storm events. Lead-210 data indicate that the upper meter of the sediment has accumulated at a rate of 3.35 to 4.71 g · cm?2 · yr?1 or approximately 8.4 to 11.8 cm · yr?1 (at ø = 0.84). Below 120 cm depth, dilution of clay and silt by low activity sand necessitates correction of the 210Pb profile in order to establish a geochronology. Grain size 210Pb distribution measurements at three depths reveal that the specific activity (dpm · g?1) of clay is 3.2 times that of silt and 24.7 times that of sand. Corrections of bulk sediment excess 210Pb activities based on these measurements lead to dates for textural changes which are consistent with charted changes in basin morphology and major storm events.Sixteen 137Cs measurements between 33–241 cm depth reveal a peak activity at 105–115 cm and indicate a minimum sedimentation rate of approximately 2.7 g · cm?2 · yr?1.  相似文献   

2.
Surface sediments of the Washington coast have 210Pb activites which average 104 ± 48dpm/g for submarine canyon and slope regimes and 18 ± 12dpm/g for the continental shelf regime. 210Pb sedimentary fluxes are also higher in canyons, averaging 18 ± 13dpm/cm2 per yr, compared to 5.2 ± 3.1 dpm/cm2 per yr for slope and 4.8 ± 1.8dpm/cm2 per year for shelf regions. These 210Pb activities and fluxes are 2–7 times greater than those reported for other coastal regions. Inputs from the atmosphere and the Columbia River are not sufficient to supply the 210Pb, but advection of seawater containing dissolved 210Pb produced in situ from 226Ra provides an input several times larger than the sedimentary fluxes. The sedimentary 210Pb flux is limited by scavenging reactions rather than by supply of dissolved 210Pb.Calculations of maximum biological uptake and fluxes of 210Pb and ‘selective’ chemical leaching experiments all show that the primary scavenging processes are due to hydrous Mn and Fe oxides rather than biological phases. The pattern of higher 210Pb depositional fluxes in canyons than in nearby open slope areas of comparable water depth is most reasonably explained by enhanced scavenging of dissolved 210Pb near the sea floor, rather than by processes operating throughout the water column. Relatively rapid removal of dissolved 210Pb from the near bottom nepheloid layer to slope and canyon sediments is shown by its mean residence time of less than two years in this layer.  相似文献   

3.
The mass balances of 210Po and 210Pb were determined for Bickford Pond, Massachusetts. Activities of these nuclides at various depths within the water column, in sediments, in streams flowing into and out of the lake and in precipitation were measured at approximately monthly intervals for a period of one year. Streamwater contained about 10 dpm/100 kg of 210Pb, mostly filtrable and showed little variation with changing flow. 210Pb in the streams is believed to be derived mostly from 222Rn that enters groundwater via alpha-recoil from aquifer matrix materials. It is therefore not meteoric in origin and represents a local source to the lake. Surface inflow was equally important as precipitation as a source of 210Pb to the lake. Only half of total 210Pb input was trapped in sediments; the rest was lost from the lake as outflow. The 210Pb removal times via scavenging and sedimentation both averaged close to 40 days and 210Pb scavenging was almost an order of magnitude greater than that of 210Po.  相似文献   

4.
210Po and 210Pb measurements of soils delineated uranium anomalies at three out of four test sites in Ontario, Canada. Measurements were made of 210Po in solutions produced by both complete digestion and partial leaching of soil samples. Direct plating of 210Po onto metal plates was followed by measuring the alpha activity. Subsequent plating of 210Po in-grown from 210Pb in solution several months later confirmed the anomalies.The 210Po and 210Pb anomalies at three of the test sites coincided with 226Ra and 222Rn anomalies. Samples from the fourth uranium occurrence associated with a known 222Rn anomaly failed to show either a 226Ra anomaly on the one hand, or 210Po or 210Pb anomalies on the other. This suggests that the 210Po and 210Pb anomalies were probably produced by the decay of 226Ra contained within secondary dispersion haloes.Although anomalies due to the 210Po and 210Pb products of 222Rn have now been documented, prospecting methods based on their use as direct tracers of the migration paths of 222Rn require much further development.  相似文献   

5.
A material balance is constructed for excess 210Pb (relative to 226Ra) as a test of the retentivity of Long Island Sound for a reactive heavy metal. Excess 210Pb is supplied to Long Island Sound chiefly by direct atmospheric deposition [1 ± 0.2(dis·min?1)cm?2·yr?1]. Rivers supply less than 20% of the atmospheric flux, and other inputs, from open ocean waters, 226Ra decay, groundwater seepage, and sewage discharge, appear to be negligible. The total input of excess 210Pb represents approximately the flux required to maintain the inventory of excess 210Pb measured in sediment cores from central Long Island Sound; that is, excess 210Pb is lost from Long Island Sound chiefly by radioactive decay. The retention of excess 210Pb within Long Island Sound is achieved in two steps: a rapid removal of soluble 210Pb onto suspended particles and the ongoing entrapment of particles in the basin by the residual bottom-water influx from the east.  相似文献   

6.
The vertical distribution of 210Pb and 210Po in the dissolved (<0.4 μm) and the paniculate (>0.4 μm) phases was measured in Crystal Lake, Wisconsin, to examine the spatial and temporal variability during the seasonal cycle of this oligotrophic lake. The concentration of unsupported 210Pb in the water column is maintained principally by atmospheric input. However, most of the 210Po in Crystal Lake is produced in situ from radioactive decay of 210Pb.Mass balance considerations indicated that the removal rates of 210Pb and 210Po from the water column to the sediment varied temporally by nearly an order of magnitude. During transient periods of high biological productivity, a large net flux of these nuclides into the sediment occurred. In addition, 210Pb was rapidly stripped from the water column during fall turnover. It was during these short-lived events that most of the annual net removal of 210Pb and 210Po occurred. The mean removal residence time was estimated to be 0.095 yr for 210Pb and 0.26 yr for 210Po. These residence times suggest that there is a difference between 210Pb and 210Po in the extent of their recycling in the water column. Calculations indicated that there was a cyclic response of the water column 210Po inventory corresponding to successive time periods where there was a net loss or net gain. This cycling is attributed to rapid biological removal and subsequent release from the sediment of freshly deposited 210Po. For 210Pb, replenishment of the water column appeared to occur mainly from atmospheric input.  相似文献   

7.
现代沉积的210Pb计年   总被引：74，自引：10，他引：74       下载免费PDF全文
万国江 《第四纪研究》1997,17(3):230-239
210Pb具有百年时间尺度沉积计年的重要价值。210Pbex计年假设：沉积物是封闭系统；进入水体的210Pb能有效地转移到沉积物中并不发生沉积后迁移；非过剩210Pb与其母体226Ra保持平衡。210Pbex计年可用稳定输入通量-稳定沉积物堆积速率模式、常量初始浓度模式或恒定补给速率模式。沉积物柱芯必须保持原态并以0．5～1cm间隔分截；用相应层节226Ra校正。沉积物表层混合作用及222Rn的丢失可能导致顶部210Pbex异常。季节性缺氧湖泊沉积物顶部可能存在210Pb及210Po的再迁移。210Pb与137Cs两种计年方法原理上具有根本差别。210Pb，137Cs与沉积纹理方法对比是准确计年的重要保证。  相似文献   

8.
Natural radionuclides in the uranium and thorium series were measured in solid tidal phases (suspended particles, bottom sediment, surface microlayer colloids) of a salt marsh in lower Delaware. The purpose was to identify potential processes responsible for trace element cycling (sources, redistribution and exchange) in salt water marshes and with their coastal waters. Generally, concentrations of U, Th,210Pb, and210Po on the tidal solid phases suggest a general mechanism by which tidal marshes appear to be trapping the nuclides into their interiors. The processes may include transport of enriched fine particles into the marsh, capture by salt marsh grass and chemical fixation by redox processes at the sediment surface. Specifically, the uranium contents of most of the samples are similar with activity ratios234U238U≧1, indicating a mixture of detrital and nondetrital (authigenic) uranium inputs such as seawater or ground water. Since the230Th daughter is generally deficient by about 50%, the authigenic enrichment process appears to favor uranium and is potentially linked to the extensive diagenetic sulfur redox cycle of salt marsh sediments. The210Po/210Pb activity ratio is less than one on Spartina adsorbed solids, and could suggest a general process in salt marshes which favors210Pb enrichment by atmospheric fallout over enrichment of210Po on time scales of weeks which correspond to complete tide marsh exchange. A228Th/232Th activity ratio of less than unity on the solids adsorbed onto marsh grass suggests a net process whereby diffusive loss of the intermediate daughter228Ra from the adsorbed solids to tidal waters dominates over potential228Th scavenging by suspended sediment.  相似文献   

9.
The Estero de Urías Lagoon (EUL) is an inner shelf barrier coastal lagoon, located in the Mexican Pacific Coast (SE Gulf of California). It is surrounded by Mazatlán City, one of the most important international tourist areas of Mexico. To provide a comprehensive reassessment of the concentration levels and spatial variability of Hg and 210Pb in the EUL, 40 surface sediment samples were analyzed for several geochemical variables (e.g. grain size distribution, organic matter and reference element concentrations) that could explain the observed variability of Hg and 210Pb. The Hg concentrations ranged from 23 to 214 ng g?1, whereas 210Pb activities varied from 20 to 56 Bq kg?1. No defined distribution pattern was observed for Hg and 210Pb concentrations in the lagoon and no evidence of a common atmospheric delivery route was observed. The sediments from EUL were found contaminated by Hg, and according to international guidelines 48 % of the sampling sites have concentrations that could be harmful to biota.  相似文献   

10.
Activity profiles of excess 234Th, excess 210Pb, 232Th, 230Th, 234U and 238U, and 228/232Th ratios determined in eight box cores of sediment from six sites in central Puget Sound provide new insights into the dynamic nature of solid phase mixing in surface sediments, the exchange of 228Ra and other soluble species across the sediment-water interface, and the cycling of U, Th and 210Pb in this coastal zone.Comparison of excess 234Th inventories in sediments with its production rate in the overlying water column indicates a mean residence time of at most 14 days for particles in the central Puget Sound water column.Surface sediment horizons with excess 234Th have no excess 228Th which might be used to ascertain sediment accumulation rates over the past decade. Instead, deficiencies of 228Th due to loss of soluble 228Ra from pore water to the overlying water persist to 20–30 cm, revealing that exchange of soluble chemicals between pore and overlying waters reaches these depths in the extensively bioturbated sediments of Puget Sound.Solid phase U isotope concentrations tend to increase by up to a factor of two with depth in sediments, as a result of dissolved U being biologically pumped down into sediments where it is partially removed when conditions become mildly reducing. 232Th and 230Th activities and 230/232Th ratios are constant with depth in sediments, indicating constant detrital phase compositions and essentially no authigenic 230Th. Steady state 210Pb depositional activities in and fluxes to Puget Sound sediments average only about onehalf those for sediments of the open Washington coast north of the Columbia River mouth, primarily because of a much lower supply of dissolved 210Pb in sea waters adverting into Puget Sound.Excess 234Th profiles in sediments reveal much more detail about the depth dependency, dynamic nature and recent history of solid phase mixing processes than excess 210Pb profiles. At least six of eight 234Th profiles show that mixing within the 210Pb-defined surface mixed layer is depth dependent. In three profiles, 234Th-derived mixing rates are fastest several centimeters below the sediment-water interface, indicating greater macro-benthic activity at these depths. Depth dependent mixing coefficients derived from the best fit of a four layer, advection-diffusion-decay model to the 234Th data are consistent with 210Pb profiles determined for the same sediments, strongly suggesting that 234Th and 210Pb are mixed equivalently and in a multilayered manner.  相似文献   

11.
 Lead-210 (210Pb) deposited from the atmosphere is used in the dating of certain geological materials such as glacial ice and lacustrine sediments, but its long-term atmospheric behavior has been little studied. The present investigation reports measurements of airborne 210Pb at 21 monitoring stations in Springfield, Missouri, during 1975–1995. Seasonal and diurnal patterns of atmospheric concentrations are established, and the mean annual concentrations of 210Pb in ground level air during the 20-year period are examined. Although airborne 210Pb concentrations are found to vary diurnally and seasonally, mean annual concentrations in southwest Missouri have remained relatively constant during this time period. This finding is important for geochronological methods that assume a constant 210Pb flux from the atmosphere. Received: 8 September 1998 · Accepted: 12 October 1998  相似文献   

12.
Vertical and temporal variations in the activities of234Th,210Po and210Pb have been measured, in both dissolved and paniculate phases, at several stations in the eastern Arabian Sea and north-central Bay of Bengal. A comparative study allows us to make inferences about the particle associated scavenging processes in these two seas having distinct biogeochemical properties. A common feature of the234Th profiles, in the Arabian Sea and Bay of Bengal, is that the dissolved as well as total (dissolved + particulate) activity of234Th is deficient in the surface 200 m with respect to its parent,238U. This gross deficiency is attributed to the preferential removal of234Th by adsorption onto settling particles which account for its net loss from the surface waters. The scavenging rates of dissolved234Th are comparable in these two basins. The temporal variations in the234Th-238U disequilibrium are significantly pronounced both in the Arabian Sea and Bay of Bengal indicating that the scavenging rates are more influenced by the increased abundance of particles rather than their chemical make-up. In the mixed layer (0–50 m), the scavenging residence time of234Th ranges from 30 to 100 days. The surface and deep waters of both the seas show an enhanced deficiency of dissolved210Po relative to210Pb and that of210Pb relative to226Ra. The deficiencies of both210Po and210Pb in the dissolved phases are not balanced by their abundance in the particulate form indicating a net loss of both these nuclides from the water column. The scavenging rates of210Po and210Pb are significantly enhanced in the Bay of Bengal compared to those in the Arabian Sea. The mean dissolved210Po/210Pb and210Pb/226Ra activity ratios in deep waters of the Bay of Bengal are ∼ 0.7 and 0.1, respectively, representing some of the most pronounced disequilibria observed to date in the deep sea. The Bay of Bengal and the Arabian Sea appear to be the regions of most intense particle moderated scavenging processes in the world oceans. This is evidenced by the gross disequilibria exhibited by the three isotope pairs used in this study.  相似文献   

13.
To determine radioactivity and trace metal levels, surface sediments were collected from two important areas (?zmir Bay and Didim) in the Aegean Sea region of Turkey, and were analyzed for concentrations of 210Po, 210Pb and trace metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn). The average 210Po and 210Pb massic activities in sediments varied in the range of 24 ± 5 to 126 ± 6 Bq kg?1 dry wt. and 18 ± 3 to 59 ± 4 Bq kg?1 dry wt., respectively. Izmir Bay exhibited the highest polonium activities in sediments, likely due to specific sedimentation processes and other sediment characteristics. The trace metal results showed that the Izmir Bay is facing trace metal pollution. The metal concentrations in sediment samples are low compared to those from the other neighboring marine environments.  相似文献   

14.
Vertical profiles of 210Po in soils near the Midwest uranium deposit and an associated surficial radioactive sandstone boulder train in northern Saskatchewan show a high 210Po background in air-dried forest litter (24 pCi/g) and Ah horizon soil (11 pCi/g) relative to lower soil horizons (<1 pCi/g). These high levels mask the 210Po signal from the radioactive boulders in the near-surface soil horizons. Only in the Bf and C horizons can the existence of the radioactive boulders be inferred from 210Po determinations. For comparative purposes profiles for 226Ra, U, Ni, and other trace elements are also presented.Escape of most of the Rn from near surface soils into the atmosphere, homogenization and decay of Rn, and precipitation of decay products back onto surface soils satisfactorily explain the field observations discussed here.Compared to the highly anomalous 222Rn signal in soil gases over this boulder train the 210Po contrast is very weak and is of little use for prospecting for this type of boulder train. The relatively high 210Po background in surficial materials relative to lower soil horizons dictates that great care be taken with the 210Po method; the deepest possible horizons should be sampled.  相似文献   

15.
The representative 210Pb and 137Cs age-depth profiles were selected from more than 100 sites in the Circum Bohai Sea (CBS) coastal region to examine the sedimentation rates and associated environmental changes. There are three unique 210Pbexc distribution patterns: 1) ideal-decaying type, representing relatively constant sediment supply and quieter environmental setting; 2) wiggling type, but with approximately equivalent amplitude, representing coarser sediments and associated stronger flow current environment; and 3) episodic-eventinfluencing type, each representing typhoon storm-influenced depositional environment. Our results also show that there is a lower sedimentation rate (ca. 0.1 cm/a) in the coastal lowlands, a higher sedimentation rate (ca. 0.5–3 cm/a) in the intertidal flat and an intermediate rate of ca. 0.58 cm/a in the subtidal zone near the Huanghua Harbor. The interbedded silt layer occurring in the core sediment reveals lower 210Pb activities, indicating a discontinuous sedimentation mostly due to typhoon events which dwarfs against 210Pb and 137Cs applicability. Overall, the 210Pb and 137Cs measurements of the present study provide physical insight into the evaluation of the coastal-marine ecological environment and associated management.  相似文献   

16.
In situ carbon flux measurements and calculated burial rates are utilized to construct an organic carbon budget for the upper meter of sediment at a single station in Cape Lookout Bight, a small marine basin located on the Outer Banks of North Carolina, U.S.A. (34°37′N, 76°33′W). Of 149 ± 20 mole · m?2 · yr?1 of total organic carbon deposited, 35.6 ± 5.2 mole · m?2 · yr?1 is recycled to overlying waters, 84 ± 18% as ∑CO2 and 16 ± 8% as CH4. Approximately 68 ± 20% of the upward carbon flux is supported by sulfate reduction while 32 ± 16% takes place as the result of underlying methanogenesis. Measured ∑CO2 and CH4 sediment-water fluxes range seasonally from 1900–6300 and 50–2500 μmole · m?2 · hr?1 respectively.The mean residence time of metabolizable organic carbon in the upper 80 cm of sediment is approximately four months with greater than 98% of the calculated total remineralization taking place within three years. In spite of large upward fluxes of methane, larger molecules derived from metabolizable sedimentary organic carbon appear to be the dominant reductants for dissolved sulfate.  相似文献   

17.
Concentrations of Al, Mn, Fe, Ag, and Pb in dissolved and particulate phases of the surface water were determined at 15 stations along the coastline off western Taiwan in April of 2007. This study presents the first set of data for Al, Ag, and Pb in the nearshore waters. Latitudinal distribution of these metals showed that high values were present in the regions affected by high fluvial discharge from the Dan-Sui River and the Cho-Sui River. Using the particle fluxes from 210Po/210Pb disequilibria, the removal fluxes and the residence times of the trace metals were calculated. Based on the K d values, the sequence of particle affinity of trace metals, Fe ~ Al >> Pb > Mn > Ag, was found. The correlation of the residence times and of the partitioning coefficients of multiple metals in the nearshore waters implies that the affinities to the particles determine the geochemical cycling of metals in the coastal water.  相似文献   

18.
Methane produced in anoxic organic-rich sediments of Cape Lookout Bight, North Carolina, enters the water column via two seasonally dependent mechanisms: diffusion and bubble ebullition. Diffusive transport measured in situ with benthic chambers averages 49 and 163 μmol · m ?2 · hr ?1 during November–May and June–October respectively. High summer sediment methane production causes saturation concentrations and formation of bubbles near the sediment-water interface. Subsequent bubble ebullition is triggered by low-tide hydrostatic pressure release. June–October sediment-water gas fluxes at the surface average 411 ml (377 ml STP: 16.8 mmol) · m?2 per low tide. Bubbling maintains open bubble tubes which apparently enhance diffusive transport. When tubes are present, apparent sediment diffusivities are 1.2–3.1-fold higher than theoretical molecular values reaching a peak value of 5.2 × 10?5 cm2 · sec?1. Dissolution of 15% of the rising bubble flux containing 86% methane supplies 170μmol · m?2 · hr?1 of methane to the bight water column during summer months; the remainder is lost to the troposphere. Bottom water methane concentration increases observed during bubbling can be predicted using a 5–15 μm stagnant boundary layer dissolution model. Advective transport to surrounding waters is the major dissolved methane sink: aerobic oxidation and diffusive atmospheric evasion losses are minor within the bight.  相似文献   

19.
210Po and 210Pb measurements of soils delineated uranium anomalies at three out of four test sites in Ontario, Canada. Measurements were made of 210Po in solutions produced by both complete digestion and partial leaching of soil samples. Direct plating of 210Po onto metal plates was followed by measuring the alpha activity. Subsequent plating of 210Po in-grown from 210Pb in solution several months later confirmed the anomalies.The 210Po and 210Pb anomalies at three of the test sites coincided with 226Ra and 222Rn anomalies. Samples from the fourth uranium occurrence associated with a known 222Rn anomaly failed to show either a 226Ra anomaly on the one hand, or 210Po or 210Pb anomalies on the other. This suggests that the 210Po and 210Pb anomalies were probably produced by the decay of 226Ra contained within secondary dispersion haloes.Although anomalies due to the 210Po and 210Pb products of 222Rn have now been documented, prospecting methods based on their use as direct tracers of the migration paths of 222Rn require much further development.  相似文献   

20.
长江河口水下三角洲210Pb分布特征及其沉积速率   总被引：5，自引：0，他引：5  
通过对长江水下三角洲采集的十个沉积物柱状样中的放射性核素210Pb分析得知,长江水下三角洲表层210Pb放射性比度在2.15~4.22 dpm·g-1之间,210Pb沉降通量在1.50~11.21 dpm·cm-2 yr-1之间,过剩210Pb总量在>48.29~>361.68 dpm·cm-2之间;210Pb沉降通量以及过剩210Pb总量均高于理论值,这表明在沉积物中存在210Pb的净输入和聚集。由210Pb放射性比度剖面所反映的沉积速率可知长江水下三角洲泥质沉积区沉积速率介于1.36~4.11 cm·yr-1之间;总体上呈现近岸沉积速率较低,沿31°N纬线向20 m等深线沉积速率升高的趋势,从122°15′E到122°30′E范围为长江水下三角洲的泥质沉积物堆积中心,其平均沉积速率为3.51 cm·yr-1。  相似文献   

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