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1.
海水中的痕量金属在海洋生物地球化学循环中至关重要。本研究在严格采用痕量金属洁净(trace-metalclean)采样和分析测试技术的前提下,于2016年7月采集了渤海与黄海表、底层海水水样,获得黄、渤海几种痕量金属(Cu、Ni、Co、Zn)的空间分布特征。研究结果显示,黄、渤海海水中痕量金属的空间分布具有近岸高、远岸低的特点,体现了人类活动对近岸海域的影响,而其在局部海域的分布则受到沿岸流、冷水团、沉积物再悬浮过程以及生物过程等因素的影响。Cu、Ni、Co在黄、渤海海水中的分布特征较为类似,平均浓度由高到低依次为渤海北黄海南黄海,而溶解态Zn的分布则与其他几种金属不同,在黄、渤海平均浓度类似,整体偏低,具有其特殊性。本研究测定的几种痕量金属在黄、渤海海水中的浓度较以往报道数据偏低,其中易污染的痕量金属Zn的浓度更是低近1—3个数量级,体现了痕量洁净采样和测试方法的重要性。  相似文献   

2.
Concentrations of dissolved Ni, Cu, Zn, Cd and Pb were measured in water samples collected during a cruise with R.V Pelagia (29-6/14-7-1993) in the northern North Sea and N.E. Atlantic Ocean. At least six depths (0–90 m) were sampled with modified Go-Flo samplers from a rubber zodiac. In the study area, the first 25 m were well mixed and stratification occurred below this depth. The local bloom of Emiliania huxleyi hardly affected the trace metals concentration, except for some removal of Cd as seen from its correlation with nitrate. The mean dissolved concentrations were for Ni (3.66 nM), Cu (1.61 nM), Zn (4.5 nM), Cd (48 pM) and Pb (108 pM). These concentrations are among the lowest reported for the North Sea and are of similar magnitude to those found in the eastern North Atlantic at the same latitude. Zn was the only exception with values 10 times higher compared to those in the Atlantic Ocean, suggesting external inputs, mainly atmospheric and possibly from surrounding land masses. The observed ratio Zn:Cd in the North Sea and estuaries is in between the high ratio 600–900 for continental sources and the low ratio 5–10 for oceanic waters. Latter low ratio is consistent with the 21-fold stronger inorganic complexation of Cd in seawater which, in combination with the preferential biological uptake of Zn, may lead to the observed about hundredfold fractionation of Zn versus Cd in the marine system. Other processes may play a role but would need further investigation. The dissolved Pb values tend to be lower than found before in the North Sea, indicating decreasing inventories due to reduced anthropogenic emissions.  相似文献   

3.
Data are presented for the concentrations of Al, Fe, Mn, Ni, Co, Cr, V, Cu, Zn, Pb and Cd in aerosols collected over two contrasting regions of the Indian Ocean. These are: (1) the northern Arabian Sea (AS), from which samples were collected in the northeast monsoon, during which the region receives an input of crustal material from the surrounding arid land masses; and (2) the Tropical Southern Indian Ocean (TSIO), a remote region from which samples were collected from air masses for which there were no large-scale up-wind continental aerosol sources. The TSIO samples can be divided into two populations: Population I aerosols, collected from air masses which have probably impinged on Madagascar, and Population II aerosols, which have been confined to open-ocean regions to the south of the area.The data indicate that there are strong latitudinal variations in the chemical signatures of aerosols over the Indian Ocean. The input of crustal material to the Arabian Sea gives rise to an average Al concentration of about 1000 ng m−3 of air in the northeast monsoon regime. As a result, the concentrations of all trace metals are relatively high, and the values of crustal enrichment factors are less than 10 for most metals, in the AS aerosols. In contrast, TSIO Population II ‘open-ocean southern air’ sampled during the southwest monsoon season, has an average Al concentration of only about 10 ng m−3 of air. Trace metal concentrations in the TSIO ‘open-ocean southern air’ during the southwest monsoon season are representative of ‘clean’ remote marine air and are generally similar to those reported over the central North Pacific.Mineral dust concentrations over the Indian Ocean decrease in a north to south direction, from about 15–20 μg m−3 of air in the extreme north to about 0.01–0.25 μg m−3 of air in the far south. The deposition of mineral dust over the northern Arabian Sea can account for approximately 75% of the non-carbonate material incorporated into the underlying sediments.In the Arabian Sea the dissolved atmospheric inputs of all the trace metals, with the exception of Cu and Co, exceed those from fluvial run-off by factors which range from 9.6 for Pb to 1.6 for Cr.  相似文献   

4.
A data base of 111 filter-collected marine atmospheric particulates is used to describe the distribution of lead over the North and South Atlantic, the Mediterranean Sea, the Red Sea, the Gulf of Aden and the northern and central Arabian Sea. The distribution of atmospheric Pb is assessed in terms of enrichment factor diagrams, and it is shown that over the marine regions studied in both the Northern and Southern Hemispheres the distribution of Pb in the atmosphere is controlled by the mixing of a background component, or components, with crustal material within certain concentration limits. For the Northern Hemisphere samples used in the investigation there is a reasonably well-defined Pb concentration minimum of ～ 0.6 ng m?3 of air; however, this will be severely decreased in more remote Northern Hemisphere marine regions. Geometric average Pb atmospheric concentrations vary from one marine region to another, ranging from ～ 0.98 ng m?3 of air for the South Atlantic westerlies to ～ 15 ng m?3 of air in the North Atlantic westerlies; although the latter reduces to ～ 7 ng m?3 of air when ‘polluted’ samples are excluded. Lead sea-surface deposition fluxes are calculated on the basis of two deposition velocities (0.25 and 1 cm s?1), the largest flux (220 ng Pb cm?2 yr?1) being found for the westerlies over the eastern margins of the North Atlantic. The distribution of lead over the North Atlantic is assessed in terms of the global lead budget and it is estimated that a maximum of ～ 24% of the total ‘natural’ lead injected annually into the World atmosphere, and ～ 3.5% of the anthropogenic lead injected annually into the Northern Hemisphere atmosphere, are deposited over the North Atlantic sea surface.  相似文献   

5.
大气输送的放射性核素7Be、210Po和210Pb,可以作为研究北冰洋大气沉降通量、海洋现代沉积以及海冰中物质传输的重要示踪剂,已被广泛应用于包括气团运动、土壤侵蚀以及水系统中颗粒物循环过程的研究。本文报道了2018年北极高纬度浮冰区表层积雪中7Be、210Po和210Pb的活度特征。7Be、210Po和210Pb的比活度变化范围分别为33.6～632.68 mBq/L、36.2～87.5 mBq/L、30.9～194.49 mBq/L。本文的研究发现,北冰洋表层积雪中7Be和210Pb比活度小于中纬度大陆地区。研究区域表层积雪中7Be的比活度随着纬度的增加而增加。此外,表层积雪中210Po/210Pb活度比值范围为0.70～1.48 (平均为0.93),210Po与210Pb活度已基本达到平衡,表明积雪样品年龄可能较“老”。  相似文献   

6.
Determinations of Zn, Ni, Mn, Cd, Cu, and Fe have been carried out on 51 near-shore and 38 open-ocean surface seawaters from various regions of the World Ocean.The concentrations of the trace metals have been established in the open-ocean waters, and have been used as “baselines” to evaluate trace-metal enhancement in near-shore regions. The factors by which the trace metals are enriched in near-shore regions vary from one element to another and, according to the highest concentration factors found, decrease in the order Zn = Mn > Cd = Cu = Ni.These elements exhibit differences in their distributions between near-shore and open-ocean waters, and they have been divided into two types on this basis: Type I, in which the largest number of samples in both shelf and open-ocean waters lie in the same concentration range. Zinc, cadmium, and copper are Type I elements. Type 2, in which the largest number of samples of near-shore waters lie in a higher concentration range than the largest number of samples of open-ocean waters. Nickel and manganese are Type 2 elements.The concentrations of Mn, Cd and Zn are similar in open-ocean surface waters from the South Atlantic and Indian Ocean, but Cu and Ni have higher concentrations in the former ocean.There is considerable variation in the concentrations of the trace metals in near-shore surface waters from various regions of the World Ocean. These variations are discussed in detail.  相似文献   

7.
We have investigated Pb concentrations and isotopic compositions in settling particles collected by sediment traps experiments over a period of two years, from May 2005 to April 2007, at two depths, 770 and 5100 m, at station KNOT in the Northwestern Pacific Ocean (44°N, 155°E). To the identify provenances of Pb, the samples were separated into two fractions by chemical leaching techniques, with the leachate expected to contain Pb of anthropogenic origin. Isotopic compositions of Pb and concentrations of Pb, Sc, Mn, La, Yb, and Th were measured by quadrupole ICP-MS. The isotope ratios of leachable Pb in settling particles were 207Pb/206Pb = 0.860 ± 0.001; 208Pb/206Pb = 2.116 ± 0.002 (mean ± 95% confidence intervals), which are similar to those of aerosols in China that are greatly affected by pollution from coal combustion. We estimated the mean contribution from anthropogenic Pb sources to the Pb in settling particles, using the conventional binary (anthropogenic and natural Pb) mixing equation for Pb isotopes, as 90% in the upper trap and 78% in the lower trap. Furthermore, we found a significant negative correlation between the isotope ratios of Pb and concentrations of leachable Mn, normalized to those of leachable Pb, suggesting that manganese oxides play an important role in transporting Pb from the upper layers of the ocean to the deeper layers. Our results support the speculation published in a previous study that Pb might be scavenged by Mn oxides in the Northwestern Pacific Ocean.  相似文献   

8.
Dissolved, weakly and strongly bound particulates Cu, Pb, Zn, Cd, Co, Ni and Fe have been measured in the surface water sampled from eleven stations in Xiamen Harbor by clean laboratory methods and GFAAS. The average concentrations found in dissolved fractions are Cu: 0.41±0.12; Pb: 0.014±0.008; Zn: 0.084±0.043; Cd: 0.022±0.004; Co: 0.009±0.004; Ni: 0.15±0.02; and Fe: 0.15± 0.02 μg/kg, which make up 62%, 6%, 12%, 85%, 5%, 25% and <1% of the total metals in the surface water respectively. The results are mucn lower than those reported previously in the coastal waters of China. Industrial sources of trace metal contamination are likely responsible for the distribution of trace metals.  相似文献   

9.
The concentrations of the clay minerals montmorillonite and illite have been determined in 28 samples of particulate material from surface (0–～5 m) waters along the eastern margins of the Atlantic Ocean, and the concentrations of chlorite and kaolinite have been determined in nineteen of the samples.The average concentration of the four clays in the particulate material decreases in the following order: illite (～42%) > kaolinite (～25%) > chlorite (～19%) > montmorillonite (～14%). There are specific trends in the latitudinal distributions of illite and kaolinite in the particulate material; illite decreases and kaolinite increases towards low latitudes. These trends are also found in eolian dusts and deep-sea sediments from the same region, and these clays are considered to have a detrital origin.The concentrations of montmorillonite in the particulate material and deep-sea sediments are similar in the North Atlantic. However, in the South Atlantic the sediments contain about twice as much montmorillonite as does the particulate material. It is suggested that whereas the montmorillonite in North Atlantic deep-sea sediments is largely detrital, that in South Atlantic sediments is both detrital and authigenic.  相似文献   

10.
The paper presents new information on the chemical composition of the insoluble aerosol fraction in the atmospheric surface boundary layer of different climatic zones of the North Atlantic (temperate humid, arid and semiarid, equatorial humid). The material for this study was collected during 12 expeditions. Nylon meshes were used to catch aerosols along the course of vessels. Aerosols above the North Atlantic consist of lithogenic, biogenic, and anthropogenic particles transported from different regions, which governs the differences in their concentrations and mineral and chemical compositions. Significant (by more than an order of magnitude) enrichment of aerosols in Cu, Cd, Zn, Pb, Sb, and Se is related to anthropogenic atmospheric pollution.  相似文献   

11.
邻近城市土壤重金属对九龙江口沉积土壤的影响   总被引：2，自引：0，他引：2  
在研究建立于漳州地区生态地球化学调查基础上，对河口湾沉积物的重金属与人口高度集中的城市地区土壤重金属的分布特征进行了对比，分析了人为活动对河口的影响，结果表明，城区与河口湾表层样品都舍有相对区域基准值较高的Hg、Cd，而且Hg富集系数要远高于Cd的富集系数。分析两种元素来源与迁移方式可知，Hg由于可通过气态形式迁移而对河口影响更大。城区与河口湾样品的重金属进行聚类分析与主因子分析结果表明：城区土壤的As、Zn、Mo、Ni、Cr和Mn主要来自基岩来源。Pb、Se、Cd可以作为人为污染的指示元素，Hg、Sn显示与其他元素具有相对独立的行为。河口湾的元素组合与城区重金属基本相似，但Pb、Cu、Se、Mo、Cd显示出两种因素都有较大影响，可以指示人为影响与基岩源的双重作用。  相似文献   

12.
In order to discuss the content distributions and fluxes of heavy metals in suspended matters during a tidal cycle in the turbidity maximum around the Changjiang(Yangtze) Estuary,the contents of heavy metals(Zn,Pb,Cd,Co and Ni) have been analyzed.During a tidal cycle,the average contents of heavy metals are in the order of ZnNiPbCo àCd.The average contents in ebb tide are generally higher than that in flood tide.However,at the inshore Sta.11,influenced by the contamination from the nearby waste treatment plant,the average contents of Zn and Ni in flood tide are higher than those in ebb tide and at the offshore Sta.10,the content of Cd in flood tide higher than that in ebb tide due to marine-derived materials.The five heavy metals,mainly terrigenous,are transported towards east-northeast,and settle down with suspended matters in the area between Sta.11 and Sta.10.Influenced by marine-derived materials,the flux value of Cd does not alter significantly with obviously changing in flux direction towards northwest.The source of heavy metals,the salinity of water and the concentration of suspended matters are the main factors controlling the content distributions of heavy metals during a tidal cycle.There is a positive correlation between the contents of heavy metals(Zn,Pb,Co and Ni) and the salinity of water,while the opposite correlation between the contents and the concentrations of suspended matters.Because of marine-derived materials,the content of Cd is not correlated with the concentration of suspended matters and the salinity of water.  相似文献   

13.
This paper presents the geochemical study of sediments along Ube, Suo-Oshima, and Kasado Bays in the Seto Inland Sea of Japan. We examined the distribution and abundances of 13 elements (As, Pb, Zn, Cu, Ni, Cr, Sr, Ca, Fe, Ti, P, Mn, and total S) in 40 coastal and river sediment samples, to evaluate the factors controlling their abundances, possible sources, and environmental implications. Average concentrations of As, Pb, Zn, Cu, Ni, and Cr at Ube were 12, 26, 86, 16, 43, and 92?mg/kg, 6, 25, 31, 8, 9, and 29?mg/kg at Kasado, and 5, 20, 28, 3, 5, and 18?mg/kg at Suo-Oshima, respectively. Average As, Pb, Zn, and Cr concentrations at Ube were comparable or enriched relative to those of the upper continental crust and Japan upper crust, whereas most major elements, Cu, and Ni were depleted at Kasado and Suo-Oshima. Enrichment factor values show low to moderate enrichment of Zn, Ni, and Cr, whereas As and Pb show significant contamination at some sites, suggesting contributions from anthropogenic sources. Anthropogenic contributions of most metals mainly originate from natural processes; however, As and Pb ranges of 73–79 and 66–81?%, respectively, confirm their anthropogenic contribution. Factor analysis and correlation matrices suggest that elevated metal concentrations at Ube, especially in samples located in the river basin, may be controlled by Fe–Mn oxy-hydroxides. Deposition of metals at Kasado and Suo-Oshima might be controlled by non-ferrous metal (i.e., aluminosilicates), sediment grain size, or source rock composition (granite and gneiss).  相似文献   

14.
Distributions of Hg, Cd, Pb, Cu and Zn in seawater and sediment from Mljet National Park, Adriatic Sea are presented for the first time. Natural and anthropogenic factors play an important role in determining resultant trace metals' concentrations in the region. We place particular emphasis on the saline “lakes” of Malo Jezero and Veliko Jezero, which have restricted flows of seawater. In Malo Jezero lake, fresh karstic spring water generated by flooding, and weathering of dolomites are the main sources of naturally elevated Cd, Pb and Zn concentrations (20.7 ± 1.6, 289 ± 19, 1260 ± 0.08 ng L?1, respectively); anthropogenic input is negligible. In Veliko Jezero lake enhanced Cu and Zn contents originate from anthropogenic input (tourism and agriculture). Distributions of the Pb and Zn in the water columns of both lakes are influenced by natural aragonite precipitation and sedimentation. Exceptionally high total Hg concentrations of 24.2 and 33.7 ng L?1 in the water column of Malo Jezero, sampled during periods of high rainfall associated with strong eastern winds, suggest an airborne input. Total Hg concentrations in waters of both lakes are elevated because of inefficient mixing. Two different metal distribution patterns exist in the sediment columns. First, Hg, Pb, Cu and Zn show elevated concentrations in recent sediments due to anthropogenic input. Second, Cd content increases with depth due to reprecipitation via a downward redox boundary shift.Described natural processes, as well as anthropogenic influence, enhance levels of trace metals. Careful study followed by suitable interpretation based on geochemical data were necessary to distinguish natural from anthropogenic sources.  相似文献   

15.
Submarine canyons represent natural conduits for preferential transport of particulate material, including anthropogenic contaminants, from coastal zones directly to the deep sea. To assess related dispersal of natural and anthropogenic lead (Pb), we analyzed Pb concentrations and stable isotope ratios in surface sediments and sediment trap particulate material from the Portuguese margin Nazaré and Setúbal/Lisbon canyons. Geochemical data are integrated with previously obtained data on near-bottom hydrodynamics and processes and pathways of sediment transport. The two canyon systems are located in close geographic proximity to each other, but represent contrasting settings in terms of sediment input and down-canyon sediment transport processes.Concentration–isotope diagrams and three-isotope plots (206Pb/207Pb vs. 208Pb/206Pb) suggest binary mixing between natural and anthropogenic end members. The inferred isotopic signature of pollutant Pb (206Pb/207Pb=1.143 [1.134–1.149, 95% confidence interval]) is most consistent with industrial Pb; ongoing influence from gasoline Pb additives is at most of minor importance. Two proposed natural end members most likely bracket the isotopic signature of natural Pb. Accordingly, binary mixing calculations indicate that on average 20–45% vs. 35–55% of total Pb is derived from anthropogenic sources in the Nazaré and Setúbal–Lisbon canyon systems, respectively. Enhanced anthropogenic influence in the latter area is consistent with its proximity to heavily populated and industrialized areas and with sediment input from the Tagus and Sado rivers, potential major carriers of pollutant particles. In both canyon systems, the anthropogenic component generally decreases with increasing water depth.Isotopic signatures of sediment trap particulate material are generally consistent with surface sediment data at similar water depth, but show large variability in the upper Nazaré canyon and major deviations from surface sediments in the lower canyon. In the lower canyon, Pb isotopic ratios of sediment trap particulate material mostly reflect low pelagic fluxes from the overlying water column, whereas surface sediment signatures are dominated by episodic down-canyon mass transport events. Such gravity flows appear to incorporate older (pre-industrial) material masking the isotopic signature of pollutant Pb. Large variability in the upper canyon reflects continuous sediment resuspension by bottom currents. Stronger average bottom currents are associated with higher 206Pb/207Pb ratios of sediment trap particulate material and hence decreased influence of pollutant Pb. This may reflect preferential resuspension of natural Pb at the canyon floor and/or additional remobilization of older, less-polluted sediment in adjacent areas such as the canyon walls.  相似文献   

16.
Samples of Mytilus californianus were analyzed to determine the spatial and temporal distribution of Ag, Al, Cd, Cr, Cu, Mn, Pb and Zn concentrations on the northwest coast of Baja California and to compare the results with levels reported for California, USA. The samples were collected at eight sites from the US-Mexican border to San Quintín, BC (300 km south of the border) in February and July 1982 and 1994. During both years, north-south gradients in the concentration of Ag and Pb were observed, with the highest values close to the US-Mexican border (Ag = 0.60-1.54 and Pb = 0.21-2.89 micrograms g-1) and the lowest in the southern part of the study area (Ag = 0.05-0.10 and Pb = not detectable-0.03 microgram g-1). The Ag and Pb gradients suggest that their distributions are affected by anthropogenic activities close to the US-Mexican border. South-north gradients in the concentration of Cd (minimum = 0.59-2.16 and maximum = 2.61-12.93 micrograms g-1), for both 1982 and 1994, were observed. The geographic annual means of Pb for California (average of six stations along the entire state) were significantly higher than those of this study (average of the eight sampling sites) in 1982 and 1994. Cu in California was significantly greater than that of this study only in 1994. Cluster analyses on all metals indicate three similar geographic zones in 1982 and 1994, suggesting a relative consistency in the processes that determine the spatial variability of the concentration of some metals in M. californianus on the northwest coast of Baja California.  相似文献   

17.
ＩＮＴＲＯＤＵＣＴＩＯＮＰｒｏｖｅｎａｎｃｅｏｆｍａｒｉｎｅｓｅｄｉｍｅｎｔｓｈａｓａｌｗａｙｓｂｅｅｎａｆｏｃｕｓｅｄｐｒｏｂｌｅｍｉｎｍａｒｉｎｅｓｅｄｉｍｅｎｔｇｅ ｏｌｏｇｙ.Ｒｅｃｏｇｎｉｔｉｏｎｏｆｅｎｄｍｅｍｂｅｒｓａｎｄｅｓｔｉｍａｔｉｏｎｏｆｔｈｅｉｒｒｅｌａｔｉｖｅｐｒｏｐｏｒｔｉｏｎｓｆｒｏｍｍｉｘｅｄｓｅｄｉｍｅｎｔｓｈａｖｅｂｅｅｎａｋｅｙｃｏｎｔｅｎｔｉｎｔｈｅｓｔｕｄｙｏｆｐｒｏｖｅｎａｎｃｅ .Ｆｏｒｔｈｉｓａｉｍ ,ｉｔｉｓｎｅｃｅｓｓａｒｙｔｏｓｅｌｅｃｔｅｎｄｍｅ…  相似文献   

18.
泉州大港湾海水、沉积物及水产生物体内重金属的含量分布   总被引：14，自引：1，他引：14  
根据1997年7月大港湾海域环境调查资料，着重分析了大港湾海水、表层沉积物及水产生物体内重金属的含量及分布。结果表明：大港湾海水中Cu，Pb，Cd，Zn的含量均低于渔业水质标准，大港湾湾顶水域，海水和表层沉积物中Cu，Pb，Cd，Zn的含最明显高于湾口水域：湾南部水域高于北部水域。文中还根据《海洋沉积物质量》、《无公害食品》、《食品中锌限量卫生标准》、《海洋生物质量》标准对表层沉积物和6种水产生物的重金属污染程度进行评价，结果大港湾的水产生物体内的重金属含量均未超标，但沉积物中的Cd含量已超标。  相似文献   

19.
Total metal concentrations in sediments from within Ensenada and El Sauzal Harbors are generally higher than at the mouths. Grain-size analyses suggested that this enrichment could be due to the presence of fine-grained sediments in the inner part of the harbors rather than to anthropogenic perturbations. The (Me/Al)(sample) ratios for Pb, Co, Ni and Fe were significantly higher for Ensenada Harbor relative to El Sauzal Harbor, whereas the ratios for Cd, Mn, Zn and Cu were statistically equivalent for both harbors. Calculated enrichment factors [EF(Me)=(Me/Al)(sample)/(Me/Al)(shale)] indicated that the metals showing slight enrichment were those associated with anthropogenic contamination (Pb, Zn), or probably related to primary productivity in the water column (Cd, Co). The levels of most of the metals were not greatly enriched, a consideration that is of the utmost importance when contamination issues are at stake.  相似文献   

20.
A wide variety of sedimentary subenvironments are found within a 10-km stretch of James River including a flood dominated channel (Rocklanding Channel) and its bank (Rocklanding Shoal), a shoal with a water depth of 1 m separating two channels (Point of Shoals), an ebb-dominated channel (Burwell Bay Channel) and its bank (Burwell Bay Bank) and a tributary (Warwick River). The concentrations of Cs-137, Cu, Pb, Zn and organic carbon in the fine-grained sediments (i.e. < 63 μm) and the amount of fine-grained sediments in eight cores covering these subenvironments were determined. The sedimentation rates, estimated by Cs-137 geochronology, range from 0·4 to > 3 cm year?1. The sedimentation rates in the Burwell Bay region are two or more, times those in the Point of Shoals and in the Rocklanding Channel and Shoal, reflecting the weaker currents in the Burwell Bay region. These sedimentation rates agree well with those obtained independently by measuring changes in the bathymetry of this area between 1873 and 1943. The concentrations of Cs-137, Cu, Pb, Zn and organic carbon in surface sediments vary by a factor of two to three. The concentrations are higher in the Burwell Bay region, probably as a result of the higher rates of accumulation of recently formed sediments in these subenvironments. The inventories of fine-grained sediments and of Cs-137, Cu, Pb, Zn and organic carbon accumulated since 1954 are also up to an order of magnitude higher in the Burwell Bay region. Although the concentrations of fine-grained sediments in three cores obtained in this region are similar, the inventories still vary by a factor of two to three. The inventories of Cs-137, Cu, Pb, Zn, organic carbon and fine-grained sediments correlate well with each other indicating that Cs-137 can be a useful tracer for studying the fate of these metals and organic carbon in estuarine environments. The inhomogeneity of the concentrations and inventories of the different elements along a 10-km segment of a river suggests that a closely-spaced sampling programme is essential for characterizing the sedimentary provinces within an estuary. The concentrations of Cs-137, metals and organic carbon in the coarse-grained sediments (i.e. > 63 μm) are considerably lower than those in fine-grained sediments. Thus, the contribution of coarse-grained sediments to the total inventory of these elements is small.  相似文献   

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