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 640 毫秒
1.
The radionuclides 210Po and 210Pb were examined to trace the cycling of particulate organic carbon (POC) and particulate organic nitrogen (PON) in the Zhubi coral reef lagoon. The net export flux of POC to the open sea is 14 mgC m−2 d−1. However, the net exchange of PON has not yet been observed. On average, the vertical export fluxes in the lagoon of POC and PON, as derived from 210Po/210Pb disequilibria, are 43 mgC m−2 d−1 and 13.8 mgN m−2 d−1, respectively. The deficit of 210Po relative to 210Pb in particulate matter provides evidence for the degradation of particulate organic matter. According to the mass balance budgets, 310 mgC m−2 d−1 and 121 mgN m−2 d−1 were recycled into dissolved fractions. Based on a first-order kinetics model, the degradation rate constants of POC and PON are 0.28 and 0.30 m−1, respectively. Thus, 210Po and 210Pb can quantify the cycling of carbon and nitrogen in this coral lagoon.  相似文献   

2.
210Po and 210Pb in mussel (Mytilus galloprovincialis) and sediment samples collected at Candarl? Gulf during the period of 2010–2012 are presented and discussed. The activity concentrations of 210Po and 210Pb were measured by means of alpha spectrometry. Activity concentrations of 210Po and 210Pb in mussels are in the ranged of 332 ± 17–776 ± 23 Bq kg−1 dw and 14 ± 1–40 ± 5 Bq kg−1 dw, for sediments the ranges for 52 ± 5–109 ± 8 Bq kg−1 dw and 38 ± 5–92 ± 9 Bq kg−1 dw, respectively. The estimated consequent annual effective ingestion dose due to 210Po and 210Pb from mussel consumption in Candarl? Gulf coastal region were calculated. The highest dose due to 210Po and 210Po were calculated to be 4232 ± 126 μSv and 126 ± 16 μSv, respectively.  相似文献   

3.
A mooring of three conical time-series sediment traps was deployed at two sites in the western Northwest Pacific Ocean for 9 months. Total mass fluxes and activities of 210Pb and 230Th were determined for the settling particles to elucidate their scavenging and transport processes. Sediment samples also were analyzed for 210Pb activities. Total mass fluxes, 210Pb fluxes and 230Th fluxes showed large seasonal variations and their weighted mean fluxes tended to increase with depth, with an especially large increase near-bottom. The ratios of the observed 210Pb fluxes to the 210Pb deficiency fluxes in the upper traps at the two sites were only 0.02 and 0.12, and were attributable to advective export of 210Pb from the surface waters. Those ratios in the near-bottom traps ranged between 1.22 and 2.63. This suggests that these high ratios are due to effective particle scavenging, large lateral 210Pb import and input of resuspended particles that have not become incorporated into the sediments. The mean total 230Th fluxes at the near-bottom traps were 4.2–6.7 times higher than that expected from production in the overlying water column. The 210Pb activities in the surficial sediments were much lower than those in the near-bottom traps. The 210Pb accumulation rates estimated from the excess 210Pb inventory in the sediment column were 40–70% higher than the mean 210Pb fluxes at the near-bottom traps. The ratios of the 210Pb accumulation rates to the 210Pb deficiency fluxes at the near-bottom traps ranged between 2.0 and 3.7. The high fluxes of particulate 210Pb and 230Th at the near-bottom traps reflected a combination of enhanced scavenging of dissolved nuclides and the lateral redistribution of particulate matter by downslope and alongshore transports. However, it was not possible to discriminate among the various processes contributing to high nuclide fluxes.  相似文献   

4.
Activities of the naturally occurring radionuclides, 210Pb and 210Po, were measured in both dissolved (<0.45 μm) and particulate (>0.45 μm) phases from surface waters of the southern South China Sea. The average activity of particulate 210Pb, 0.23 Bq/m3 (n=23), accounted for about 12% of the total 210Pb, which corresponds with values of open oceans. Particulate 210Po, with an average activity of 0.43 Bq/m3, accounted for about 40% of the total 210Po, which was much higher than those of open and eutrophic oceans. The residence times of total 210Po and 210Pb in surface waters estimated from an irreversible steady-state model were 0.82 a and 1.16 a, respectively. The consistently high fractionation factor calculated either by scavenging rate constants (5.42) or Kd values (6.69) suggested that a significant fractionation occurred between 210Po and 210Pb during their removal from solution to particles and that the two radionuclides had different biogeochemical cycling pathways in the oligotrophic South China Sea. Furthermore, our results indicated that there exist different fractionation mechanisms between 210Po and 210Pb in different marine environments: in eutrophic ocean, plankton detritus and fecal pellets are the main carrier of 210Po and 210Pb, by which 210Po and 210Pb have been scavenged and removed; while in oligotrophic ocean, microbes could become the main carrier of 210Po and fractionate 210Po and 210Pb significantly as a result of scarce plankton detritus and fecal pellets. These results suggest the use of 210Po to trace marine biogeochemical processes relating to microbial activities and the cycling of sulfur group elements (S, Se, Te and Po).  相似文献   

5.
The activities of 210Po and 210Pb were determined in commonly consumed seafoods to evaluate the internal exposure and risk to humans residing Kudankulam coast where a mega nuclear power plant is under construction. The concentration of 210Po in seafoods ranged from 1.2 ± 0.7 to 248 ± 8.1 Bq kg−1. Meanwhile, 210Pb ranged between 1.1 ± 0.05 and 14.8 ± 1.6 Bq kg−1. The committed effective dose (CED) due to 210Po and 210Pb varied from 11.04 to 515.6 and 3.93 to 23.5 μSv yr−1, respectively. The lifetime cancer risk for the public due to 210Po was in the range of 3.47 × 10−5-1.62 × 10−3 and it was 4.03 × 10−5-1.96 × 10−4 due to 210Pb. The activity intake, effective dose and cancer risk was found lesser than international guidelines and the seafood intake was considered to be safe for human consumption.  相似文献   

6.
Profiles of226Ra and dissolved210Pb have been measured at several stations in the Red Sea. At one station in the central Red Sea an expanded profile was measured including226Ra and dissolved and particulate210Pb and210Po. These profiles show several distinct features: (1)226Ra displays a mid-depth maximum of about 13 dpm/100 kg at about 500 m; (2) dissolved210Pb concentrations are uniformly low at about 2 dpm/100 kg with little lateral or vertical variation; (3) the surface-water210Pb excess which is commonly observed in low-latitude open ocean regions is entirely lacking; (4)210Pb and210Po activities are essentially identical to each other in both particulate and dissolved phases although210Po activities appear somewhat lower; (5) about 20% of the210Pb and210Po in the water column residues on particulate matter.Assuming the atmospheric210Pb flux to be in the dissolved form and at the lower level of the normal range i.e. 0.5 dpm/cm2 yr, the residence time of the dissolved Pb is about 1.5 years. However, if the same atmospheric flux is entirely in particulate form, then the residence time of the dissolved Pb is about 5 years. The residence time of Pb in the particulate phase is less than 0.4 years if all the Pb is removed only by sinking particles.  相似文献   

7.
226Ra,210Pb and210Po were measured in oceanic profiles at two stations near the Bonin and Kurile trenches.210Po is depleted by 50% on average relative to210Pb in the surface water. In the deep water,210Pb is about 25% deficient relative to226Ra. Based on the deficiency,210Pb residence time with respect to removal by particulate matter was estimated to be less than 96 years in the deep water.210Pb deficiency in the bottom water was significantly greater than that of the adjacent deep water, indicating more effective removal near or at the bottom interface.210Pb,210Po and Th appear to have similar overall rate constants of particulate removal throughout the water column.  相似文献   

8.
Naturally occurring 210Po (half-life 138.4d) is the granddaughter of 210Pb (half-life 22.3a), both are members of 238U decay series and have been inten-sively utilized to study kinetic aspects of material cy-cling in the ocean[1]. Based on radioactive disequilibria in the 226Ra-210Pb-210Po system, oceanographical processes with different timescales have been widely studied. Rama et al.[2] first detected excess 210Pb rela-tive to its precursor 226Ra in surface waters, and considered this exc…  相似文献   

9.
The progressive weakening and final disappearance (in 1979) of the long-term meromictic structure of the Dead Sea are clearly reflected in the depth profiles of210Pb and210Po. In 1977/78, prior to overturn, dissolved210Pb (35–50 dpm kg?1) predominated over particulate210Pb (1–2 dpm kg?1) in the oxic upper waters, whereas the reverse was true in the anoxic deep waters (16–20 dpm kg?1 particulate vs. 2–5 dpm kg?1 dissolved). The exact extent of the disequilibrium between210Pb and226Ra is hard to evaluate in the upper oxic layers, because the progressive deepenings resulted in mixing with deep waters. By contrast, one can estimate the residence time of dissolved210Pb in the unperturbed anoxic deepest layers, because these remained isolated, at about 3 years. Following the overturn of 1979, dissolved210Pb exceeded particulate210Pb at all depths. The210Po profiles of the stratified lake resembled in shape those of its grandparent210Pb, but with distinct characteristics of their own in the oxic upper waters where particulate210Po (8–12 dpm kg?1) was greatly in excess over particulate210Pb, while dissolved210Po (25–40 dpm kg?1) was slightly deficient. Immediately following the overturn, dissolved and particulate210Po were similar (about 15 dpm kg?1), at all depths. The destruction of the lake's meromictic structure was accompanied by a reduction of its210Pb inventory, while that of210Po was almost unaffected. Thus, at overturn a transient state was created with the inventory of210Po exceeding that of210Pb.  相似文献   

10.
The distribution of210Po and210Po in dissolved (<0.4 μm) and particulate (>0.4 μm) phases has been measured at ten stations in the tropical and eastern North Atlantic and at two stations in the Pacific. Both radionuclides occur principally in the dissolved phase. Unsupported210Pb activities, maintained by flux from the atmosphere, are present in the surface mixed layer and penetrate into the thermocline to depths of about 500 m. Dissolved210Po is ordinarily present in the mixed layer at less than equilibrium concentrations, suggesting rapid biological removal of this nuclide. Particulate matter is enriched in210Po, with210Po/210Pb activity ratios greater than 1.0, similar to those reported for phytoplankton. Box-model calculations yield a 2.5-year residence time for210Pb and a 0.6-year residence time for210Po in the mixed layer. These residence times are considerably longer than the time calculated for turnover of particles in the mixed layer (about 0.1 year). At depths of 100–300 m,210Po maxima occur and unsupported210Po is frequently present. Calculations indicate that at least 50% of the210Po removed from the mixed layer is recycled within the thermocline. Similar calculations for210Pb suggest much lower recycling efficiencies.Comparison of the210Pb distribution with the reported distribution of226Ra at nearby GEOSECS stations has confirmed the widespread existence of a210Pb/226Ra disequilibrium in the deep sea. Vertical profiles of particulate210Pb were used to test the hypothesis that210Pb is removed from deep water by in-situ scavenging. With the exception of one profile taken near the Mid-Atlantic Ridge, significant vertical gradients in particulate210Pb concentration were not observed, and it is necessary to invoke exceptionally high particle sinking velocities to account for the inferred210Pb flux. It is proposed instead that an additional sink for210Pb in the deep sea must be sought. Estimates of the dissolved210Pb/226Ra activity ratio at depths greater than 1000 m range from 0.2 to 0.8 and reveal a systematic increase, in both vertical and horizontal directions, with increasing distance from the sea floor. This observation implies rapid scavenging of210Pb at the sediment-water interface and is consistent with a horizontal eddy diffusivity of 3?6 × 107 cm2/sec. The more reactive element Po, on the other hand, shows evidence of rapid in-situ scavenging. In filtered seawater,210Po is deficient, on the average, by ca. 10% relative to210Pb; a corresponding enrichment is found in the particulate phase. Total inventories of210Pb and210Po over the entire water column, however, show no significant departure from secular equilibrium.  相似文献   

11.
The concentrations of radionuclides of the U-Th series (238U,234Th,234U,230Th,226Ra,210Pb,210Po, and232Th,228Ra,228Th) in the water of Narragansett Bay are reported. Analysis of the total, particulate, dissolved and colloidal forms of Th isotopes reveal a consistent removal behavior which is controlled mainly by the particulate matter concentration and the sediment resuspension rate. Half-removal times of Th from solution onto particles range from 1.5 to 15 days, and settling velocities of Th containing particles range generally between 1 and 11 m/day.210Pb and210Po concentrations are seasonally dependent, with higher concentrations and slower removal during the early summer (half-removal times from solution onto particles of 1–5 days in winter and up to 2 months in early summer).  相似文献   

12.
Disequilibrium between210Po and210Pb and between210Pb and226Ra has been mapped in the eastern and central Indian Ocean based on stations from Legs 3 and 4 of the GEOSECS Indian Ocean expedition.210Po/210Pb activity ratios are less than 1.0 in the surface mixed layer and indicate a residence time for Po of 0.6 years.210Po and210Pb are generally in radioactive equilibrium elsewhere in the water column except at depths of 100–500 m, where Po may be returned to solution after removal from the surface water, and in samples taken near the bottom at a few stations.210Pb excesses relative to226Ra are observed in the surface water but these excesses are not as pronounced as in the North Pacific and North Atlantic. The difference is attributable to a lower flux of210Pb from the atmosphere to the Indian Ocean. Below the main thermocline,210Pb activities increase with depth to a broad maximum before decreasing to lower values near the bottom. Departures from this pattern are especially evident at stations taken in the Bay of Bengal (where210Pb/226Ra activity ratios as low as 0.16 are observed) and near the Mid-Indian Ridge. The data suggest that removal of210Pb at oceanic boundaries, coupled with eddy diffusion along isopycnals, can explain gradients in210Pb near the boundary. Application of a simple model including isopycnal diffusion, chemical removal, production and radioactive decay produces fits the observed210Pb/226Ra gradients for eddy diffusion coeffients of ～ 107 cm2/s. High productivity in surface waters of the Bay of Bengal makes this region a sink for reactive nuclides in the northern Indian Ocean.  相似文献   

13.
By modelling the observed distribution of210Pb and210Po in surface waters of the Pacific, residence times relative to particulate removal are determined. For the center of the North Pacific gyre these are τPo = 0.6years andτPb = 1.7years. The surface ocean τPb is determined by particulate transport rather than plankton settling. The fact that it is about two orders of magnitude smaller than τPb for the deep ocean implies a sharp change in the adsorptive quality of particles during descent through the water column.  相似文献   

14.
Measurements have been made of226Ra and both dissolved and particulate forms of210Pb and210Po in a vertical profile at 85°50′N, 108°50′W in the Arctic Ocean.In the upper water column226Ra shows a concentration maximum that is coincident with one in the nutrients, silicate, phosphate, and nitrate, while at the same depth, dissolved and particulate210Pb and210Po all show minimum concentrations. It is suggested that the concentration maxima are partly due to sources of the respective elements in the continental shelf sediments, the shelf waters being subsequently advected into the Arctic Ocean basins. The210Pb and210Po minima have similarly been explained by interaction between the shelf sediments and overlying waters. An estimate is made of the possible contributions of shelf sediments to the layer of silica-rich water which covers the Canada Basin at a depth of 100–150 m.Residence times have been calculated for dissolved210Pb and210Po at various depths in the water column. Surface water residence times of dissolved and particulate forms of these radionuclides are longer than in surface Atlantic waters, probably due to lower biological activity in the surface waters of the Canada Basin. An estimatee has been made of the average sinking velocity of particulate material.  相似文献   

15.
Two ocean profiles from the Peru Basin from regions with different surface productivities were analyzed for total210Pb and201Po to evaluate the influence of particulates in the water column on their distribution. Comparison with a published226Ra profile for the region was made. The profile closest to the coast, where upwelling and productivity are high, shows depletion of210Pb relative to226Ra at all depths, with particularly marked excursions from radioactive equilibrium at the surface and in the bottom water.210Po appears to be deficient relative to210Pb at depth as well. Mean residence times in the deep water, relative to particulate removal from the water column to the sediments, of about 100 years for210Pb and about two years for210Po are indicated. The profile northwest of the upwelling region shows the226Ra210Pb210Po system close to equilibrium at all depths to 1500 m (except for the effect of atmospheric210Pb input seen at the surface.  相似文献   

16.
The 210Pb dating method was first introduced by Goldberg (1963), and since then has been applied to study sediment from lakes, estuaries and coastal marine environments. Hundreds of studies around the world have used 210Pb as a geochronological tool in aquatic ecosystems. However little attention has been paid to the potential of this naturally occurring isotope as an environmental tracer of ecological events. Here we report three instances in which 210Pb profiles measured on undisturbed sediment cores from lakes, rivers and fjords show us the potential of 210Pb profile as a tracer of natural and anthropogenic processes. The methodology used here is a suite of techniques combining biogeochemistry (micro-electrodes), paleomagnetism (susceptibility), sediment characteristics (LOI) and visualization (SPI and X-ray) applied to the interpretation of 210Pb profiles. We measured 210Pb profiles on sediments from a river, Cruces River (Chile), which recorded a clear shift in the water chemistry caused by a pulp mill effluent to the river. Here metal mobilization and remobilization of the tracer may be the cause of the observed profile. We also measured 210Pb profiles in sediment from two fjords of Southern Chile (Pillan and Reñihue), the sudden deposition change of fresh 210Pb with depth observed could very well be the result of bioturbation but it occurred in a seafloor area deprived of bioturbators. In this case, 210Pb recorded the onset of aquaculture activities (fish farming) that took place two decades ago. Finally, 210Pb profiles measured in two lakes in the “pampa Argentina”: Epecuen and Venado showed a particular shape with depth. These profiles apparently registered a sudden depositional event with recent 210Pb material, probably related to strong shifts in precipitation and drought cycles in that part of the world. These three examples show that 210Pb profiles provide valuable information not only on geochronology, but also related to natural and anthropogenic short term processes, as shown here, but these are not always reported and well understood.  相似文献   

17.
210Pb is widely used for dating recent sediments in the aquatic environment; however, our experiences working in shallow coastal environments in the Pacific coast of Mexico have demonstrated that the potential of 210Pb for reliable historical reconstructions might be limited by the low 210Pb atmospheric fallout, sediment mixing, abundance of coarse sediments and the lack of 137Cs signal for 210Pb corroboration. This work discusses the difficulties in obtaining adequate sedimentary records for geochronological reconstruction in such active and complex settings, including examples of 210Pb geochronologies based on sediment profiles collected in two contrasting areas coastal areas (mudflats associated to coastal lagoons of Sinaloa State and the continental shelf of the Gulf of Tehuantepec), in which geochemical data was used to support the temporal frame established and the changes in sediment supply recorded in the sediment cores which were related to the development of land-based activities during the last century.  相似文献   

18.
湖泊沉积记录研究对了解流域侵蚀、揭示区域气候环境变化及人类活动影响、建立外生地球化学循环模式等均具有重要意义.放射性同位素~(210)Pb和~(137)Cs组合定年法是百年尺度湖泊沉积记录研究的首选方法,在过去几十年中得到了广泛应用,大力推动了湖泊沉积记录的高分辨率气候环境变化研究的开展.然而,如何理解和选择适用的计算模式来尽可能地提高定年准确度目前仍存在争议,这在一定程度上限制了该方法的应用.鉴于上述问题,本文基于本实验室近年来从青藏高原获取的若干支代表性湖芯的定年结果,从样品前处理、仪器及测试、数据分析及计算等全过程对~(210)Pb、~(137)Cs定年原理和方法进行了较为系统的阐述;在此基础上,提出了~(210)Pb定年样品封装原则,探讨了高纯锗γ谱仪在放射性活度测量中的影响因素,并建立了准确有效的比活度校正方法;明确指出了恒定初始浓度模式(constant initial concentration,CIC)可用于计算沉积物每层的年龄,而不是部分研究中认为的平均沉积速率,这对于深刻理解该定年模式并提供准确的定年结果具有重要的参考意义.同时,通过对比两种放射性核素的分布特征发现,相对于~(210)Pb而言,~(137)Cs更容易发生垂向迁移进而影响其时标准确性,这需引起研究者的充分重视,因此,当二者定年结果出现明显差异时,建议以~(210)Pb定年结果为准.  相似文献   

19.
The radionuclides (210)Po and (210)Pb were examined to trace the cycling of particulate organic carbon (POC) and particulate organic nitrogen (PON) in the Zhubi coral reef lagoon. The net export flux of POC to the open sea is 14 mg Cm(-2) d(-1). However, the net exchange of PON has not yet been observed. On average, the vertical export fluxes in the lagoon of POC and PON, as derived from (210)Po/(210)Pb disequilibria, are 43 mg Cm(-2) d(-1) and 13.8 mg Nm(-2) d(-1), respectively. The deficit of (210)Po relative to (210)Pb in particulate matter provides evidence for the degradation of particulate organic matter. According to the mass balance budgets, 310 mg Cm(-2) d(-1) and 121 mg Nm(-2) d(-1) were recycled into dissolved fractions. Based on a first-order kinetics model, the degradation rate constants of POC and PON are 0.28 and 0.30 m(-1), respectively. Thus, (210)Po and (210)Pb can quantify the cycling of carbon and nitrogen in this coral lagoon.  相似文献   

20.
The fundamental assumption of 210Pb sediment dating is the stable flux of 210Pbex, which was derived from atmosphere and then transferred into sediments via lake water. When the sedimentation rate is relatively constant, the 210Pbex activity in sediments will be exponentially reduced with sedimentation age. 210Pbex in lake water is incorporated into sediments mainly via organic particulates. If the sedimentation flux of organic matter in lake water is suddenly increased, 210Pbex will be significantly deposited and then transferred into sediments. On the one hand such sudden purification effect is obviously unfit for the fundamental assumption of 210Pb dating; on the other hand, the sudden enhancement of 210Pbex flux would be indicative of the conspicuous variation of primary productivity of lake water. This problem will be discussed in accordance with the variation trend of 210Pbex in the vertical profile of recent sediments of Lake Chenghai, Yunnan Province. The sediment core was collected from the deep-water area of Lake Chenghai in June 1997. The vertical profile of 137Cs activity is characterized by a tree-peak pattern. This profile gave reliable ages, and also showed the stability of sediment accumulation in the recent ten years. The vertical profile of 210Pbex activity displays a specific distribution of peaks, and is similar to the vertical profile of Corg. This phenomenon seems to be related to the mechanism of constraining the transfer of 210Pbex into lake sediments. The average atomic ratios of Horg/Corg and Corg/Norg in Lake Chenghai sediments are 5.51 and 7.04, respectively, indicating that the organic matter was predominantly derived from the remains of endogenic algae. In terms of the three-stage evolutionary characteristics of organic matter in sediments, i.e., “deposition-de-composition-accumulation”, the sedimentation fluxes (F(Corg)) of organic carbon (Corg) since 1970 were calculated by modeling. The sedimentation fluxes of 210Pbex (F(210Pbex)) in different years display good synchronous relations with the sedimentation flux of organic carbon (F(Corg)), especially in the years of 1972–1974 and 1986–1989. The variation of F(Corg) led to the variation of F(210Pbex); the variation of F(210Pbex) reflects, to some extent, the historical variation of lake productivity.  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