共查询到20条相似文献，搜索用时 403 毫秒
1.
Lutz Brügmann 《Marine Chemistry》1988,23(3-4)
Between 1980 and 1984 extensive studies were carried out in the Baltic Sea on trace metals (Cd, Co, Cu, Fe, Hg, Mn, Ni, Pb and Zn) in water, suspended matter and sediments. The results enabled the influence of different factors on metal distribution patterns to be considered. The vertical profiles of dissolved and particulate metals in waters of the central deep basins reflect influences caused by oxygen deficiency and anoxic conditions in near-bottom water layers. Peculiarities at Station BY15 in the Gotland Deep included high dissolved Fe, Mn and Co concentrations and remarkable enrichment of Zn (0.64%), Cd (51 μg g−1) and Cu (0.15%) in particulate matter from the anoxic zone. Manganese-rich particles were accumulated above this layer.In fine-grained soft sediments below anoxic deep waters, maximum contents of Cd, Cu and Zn were observed, relative to other coring sites, between Bothnian Bay and Lübeck Bight. The Hg content in sediments probably reflects the joint flocculation with organic matter. Land-based sources seem to play the leading part for maximum lead contents. 相似文献
2.
3.
孔隙水是沉积物-海水界面链接沉积物颗粒和上覆水体的一个重要过渡相态,针对其研究可更好地了解痕量金属在固-液界面的早期成岩过程。近年来,针对孔隙水中痕量元素研究的方法较为匮乏,为此建立了一种分析测定海洋沉积物孔隙水中7种痕量金属元素(Mn、Cu、Zn、Ni、Cd、Co、Pb)的方法,该方法使用Nobias PA1树脂进行富集分离,再使用电感耦合等离子体质谱(ICP-MS)进行测试,可针对孔隙水中的痕量金属元素进行准确分析。通过实验结果发现该方法最优实验条件为: Nobias PA1树脂富集时的pH值为5.5~6.0,洗脱酸浓度为1.3 mol/L硝酸,体积为1 mL。同时,样品需进行紫外消解4 h以上以分解有机络合物,该消解步骤对Cu和Co这两种元素尤其重要。该方法通过加标回收获得Mn、Cu、Ni、Co和Pb的回收率在92%~100%, Zn和Cd的回收率分别为72%和82%; Mn、Cu、Zn、Ni的方法检出限范围为0.03~0.53 nmol/L, Cd、Co、Pb的方法检出限范围为2.66×10-3~8.60×10-3 nmol/L,满足孔隙水中痕量金属浓度的测试需求。同时,根据检出限计算的结果显示,孔隙水样品只需1 mL,即可应用该方法进行测试。应用该方法测试了一根采集于北黄海中部沉积物短柱的孔隙水样品,测试结果显示其垂相分布合理、较符合早期成岩过程规律。此研究为分析海洋沉积物孔隙水中痕量金属元素提供了一种准确而简便的方法。 相似文献
4.
Baltic surface water was sampled at a fixed position at intervals of a few hours. The trace metal concentrations were measured by graphite furnace AAS after extraction. The mean concentrations found were (ng l?1): Cd, 30 ± 2.7; Cu, 800 ± 48; Fe, 358 ± 165; Ni, 820 ± 49; Pb, 16 ± 4.5; Zn, 900 ± 160. The variability in the trace metal concentrations is of the same order of magnitude as the precision of the method. Thus, no spatial variations in trace metal concentrations were found. 相似文献
5.
The contents of Fe, Mn, Cu, Co, Ni, Pb and Zn in the seaiment associated with manganese nodules from the Northern Central Pacific Ocean and in their acid-soluble fractions were determined and correlations among the elements and between the trace metals and environmental parameters were discussed. It has been found that the contents of Mn, Cu and Ni in the sediment are one order of magnitude higher than those in the common sediment. As shown in the manganese nodules, they may mainly derive from seabed. The contents of all trace metals in the sediment are obviously governed by Fe-and Mn-oxides, organic matter, seawater depth, particle size and Eh. Multi-element correlation equations were developed for all trace metals. The trace metals in acid-soluble fraction of the sediment were also much higher than ihose of common sediment and negatively correlated with water depth, implying the possible influence of carbonate speciation. 相似文献
6.
Murat
ztürk 《Marine Chemistry》1995,48(3-4)
Anoxic sulfidic waters provide important media for studying the effect of reducing conditions on the cycling of trace metals. In 1987–1988, dissolved and particulate trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) concentrations were determined in the water column of the anoxic Drammensfjord basins, southeastern Norway. The iminodiacetic acid type chelating resin (Chelex 100) was used for the preconcentration of trace metals. The trace metal concentrations were determined using atomic absorption spectrophotometry (AAS), differential pulse polarography (DPP), and differential pulse-anodic stripping voltammetry (DP-ASV).It was observed that the trace metals Mn and Fe were actively involved in the processes of redox cycling (oxidationreduction and precipitation-dissolution) at the O2/H2S interface. The dissolved concentrations of Mn, Fe and Co showed maxima just below the O2/H2S interface. The seasonal enhancement in the maxima of both dissolved and particulate Mn and Fe at the redox cline is mainly governed by the downward movement of water which carries oxygen. An association of Co with the Mn cycle was observed, while the total dissolved Ni was decreased by only 10–35% in the anoxic waters. The dissolved concentrations of Cu, Zn, Pb and, to a lesser extent, Cd decreased in the anoxic zone. 相似文献
7.
The present study was undertaken for assessing the level of heavy metals such as iron, manganese, zinc, copper, nickel, cadmium, lead, and cobalt in recent sediment samples of Safaga Bay, Egypt. Concentration of heavy metals in sediments shows significant variability and ranges from 863.37 to 1144.93 ppm for Fe, 64.29–586.8 ppm for Mn, 2.7–12.68 ppm for Zn, 3.01–7.2 ppm for Pb, 1.53–3.29 ppm for Ni, 0.55–1.57 ppm for Co, 0.16–1.37 ppm for Cu, and 0.22–0.4 ppm for Cd. Sediment pollution assessments were carried out using an enrichment factor and geoaccumulation index. The calculation of enrichment factor showed that Cd is enriched by 4.1 due to phosphate sources in Safaga Bay. The Geoaccumulation index results revealed that there are positive and negative correlations between Fe, Zn, Mn, Pb, Ni, Cu, Co, and Cd indicating that these metals have complicated geochemical behaviors. 相似文献
8.
《Deep Sea Research Part II: Topical Studies in Oceanography》2009,56(26):2822-2838
During mesoscale Fe enrichment (SEEDS II) in the western North Pacific ocean, we investigated dissolved and particulate Co, Ni, Cu, Zn, Cd and Pb in seawater from both field observation and shipboard bottle incubation of a natural phytoplankton assemblage with Fe addition. Before the Fe enrichment, strong correlations between dissolved trace metals (Ni, Zn and Cd) and PO43−, and between particulate trace metals (Ni, Zn and Cd) and chlorophyll-a were obtained, suggesting that biogeochemical cycles mainly control the distributions of Ni, Zn and Cd in the study area. Average concentrations of dissolved Co, Ni, Cu, Zn, Cd and Pb in the surface mixed layer (0–20 m) were 70 pM, 4.9, 2.1, 1.6, 0.48 nM and 52 pM, respectively, and those for the particulate species were 1.7 pM, 0.052, 0.094, 0.46, 0.037 nM and 5.2 pM, respectively. After Fe enrichment, chlorophyll-a increased 3 fold (up to 3 μg L−1) during developing phases of the bloom (<12 days). Mesozooplankton biomass also increased. Particulate Co, Ni, Cu and Cd inside the patch hinted at an increase in the concentrations, but there were no analytically significant differences between concentrations inside and outside the patch. The bottle incubation with Fe addition (1 nM) showed an increase in chlorophyll-a (8.9 μg L−1) and raised the particulate fraction up to 3–45% for all the metals, accompanying changes in Si/P, Zn/P and Cd/P. These results suggest that Fe addition lead to changes in biogeochemical cycling of trace metals. The comparison between the mesoscale Fe enrichment and the bottle incubation experiment suggests that although Fe was a limiting factor for the growth of phytoplankton, the enhanced biomass of mesozooplankton also limited the growth of phytoplankton and the transformation of trace metal speciation during the mesoscale Fe enrichment. Sediment trap data and the elemental ratios taken up by phytoplankton suggest that export loss was another reason that no detectable change in the concentrations of particulate trace metals was observed during the mesoscale Fe enrichment. 相似文献
9.
研究了珠江口贫氧区表层沉积物中Cu,Pb,Zn,Cd,Fe和Mn含量的相互关系;探讨它们在迁移和固-液平衡过程相互作用的特征;研究了沉积物的环境因素和重要组分对其沉积-溶解作用的影响;研究了表层沉积物对它们的富集作用。结果发现,沉积物对Cu,Pb,Zn和Cd的富集系数(K)排列次序为K_(Cd)>K_(Pb)>K_(Cu)>K_(Zn)。K_(Cd)大于对照区和长江口的相应值。此结果说明,上述区域的表层沉积物中可能有自生的CdS。且贫氧水的表层沉积物中Fe,Mn,Cu,Pb和Cd的地球化学特性尚未有显著的改变。 相似文献
10.
Lars-Göran Danielsson Bertil Magnusson Stig Westerlund Kerong Zhang 《Estuarine, Coastal and Shelf Science》1983,17(1):73-85
The concentrations of the trace metals Cd, Cu, Fe, Ni, Pb and Zn in the Göta River estuary have been investigated. The following metal fractions have been determined: acid-leachable, dissolved, labile and particulate.The estuary represents a salt wedge type estuary and is situated in a densely populated region of Sweden. The metal concentrations found for the dissolved fraction is in the range of what can be considered as background levels for freshwater. It is difficult to evaluate any estuarine processes other than conservative mixing for Cd, Cu, Ni and Zn. The dissolved levels in the freshwater end member are Cd, 9–25 ngl?1; Cu, 1·1–1·4 μgl?1; Fe, 20–75 μg l?1: Ni, 0·7–0·9 μg l?1: Pb 0·09–0·2 μg l?1; and Zn, 6–7 μg l?1:The results from the acid-leachable fraction show that at high suspended load the particles sediment in the river mouth. The trace metal levels in this fraction are subject to large variations. 相似文献
11.
We report a simplified synthesis, and some performance characteristics, for 8-hydroxyquinoline (8-HOQ) covalently bonded to a chemically resistant TosoHaas TSK vinyl polymer resin. The resin was used to concentrate trace metals from stored, acidified seawater samples collected from Jellyfish Lake, an anoxic marine lake in the Palau Islands. The Mn, Fe, and Zn profiles determined from the 8-HOQ resin extraction were similar to those determined using Chelex-100 resin. The Zn and Cd profiles did not exhibit removal by sulfide “stripping” in contrast to other anoxic marine basins. The profiles of Co and Ni also exhibited elevated concentrations in the anoxic hypolimnion. The solution speciation and saturation states for the metals were calculated using revised metal-bisulfide stability constants. The calculations suggest that the MS(HS)− species dominates the solution speciation for Mn, Co, Ni, Zn, Cd, and Pb. Cu(I) is modeled as the CuS− or Cu(HS)2− species, while Fe(II) behaves as the free Fe2+ cation. The Mn, Co, Ni, Cu and Cd concentrations appeared to be at least 10-fold undersaturated, while the Fe(II), Zn, and Pb concentrations were close to saturation with respect to their metal sulfides. 相似文献
12.
An investigation of trace metal distributions in the Western Mediterranean Sea was carried out during the RRS Discovery cruise (July 1993) in which a transect from the Strait of Gibraltar to the Strait of Sicily was conducted. Organically complexed dissolved trace metals and their total concentrations were measured to investigate the end-members and to predict the environmental capacity of the Mediterranean for potential toxic metals. The distribution of trace metals can be accounted for by the mixing of several end-members and by some atmospheric inputs to the surface water. For Pb and Fe, the effects of the atmospheric inputs are more pronounced than for the other metals. Due to the rapid exchange of water masses, the Western Mediterranean may have the ability to assimilate the increased external inputs for some trace metals such as Cu, Cd, Ni and Zn. But the external inputs for Pb and Fe exceed the removal capacity of the Western Mediterranean and these elements may accumulate in the water column of the western basin. The C18 Sep-Pak technique and direct determination by DPASV were used to determine the amount of trace metal–organic complexes. The C18 Sep-Pak column isolates only a small fraction of trace metals except for Cu. The maximum hydrophobic fractions for the studied trace metals, except for Cd and Pb, which are not detectable, were found in the subsurface layer at all stations. This maximum may well be linked to picoplankton activity and the picoplankton, prochlorophytes may have an important role in the speciation of dissolved Cu as well as Synechococcus. These organic ligands for Cu were produced at the maximum of biological activity in the Western Mediterranean basin and seem to be accumulated at halocline level by Mediterranean hydrodynamic characteristics. However, direct determination by DPASV showed that the major part of Cu, Cd and Pb, complexed by organic materials, was not isolated by C18 Sep-Pak technique. 相似文献
13.
Environmental status of Daya Bay surface sediments inferred from a sequential extraction technique 总被引：1，自引：0，他引：1
Xuelu Gao Chen-Tung Arthur Chen Gang Wang Qinzhao Xue Cheng Tang Shaoyong Chen 《Estuarine, Coastal and Shelf Science》2010,86(3):369-378
The chemical partitioning of 12 trace metals (Ba, Cd, Co, Cu, Mn, Mo, Ni, Pb, Sc, Sr, U, Zn) in 9 surface sediments from Daya Bay, northern South China Sea, was studied by a four-step sequential extraction technique to assess their environmental/pollution status. The studied metals take on different fraction composition patterns, and some of them show significant spatial variation especially for Cd. A majority of the studied metals can be considered immobile because of their high percentages in the residual fraction. It seems that the Daya Bay surface sediments have not yet been polluted by the studied heavy metals which are used as parameters to classify marine sediment quality, i.e., Cd, Cu, Ni, Pb and Zn. For all metals except for Pb, the extent of anthropogenic influences on their total concentrations in the Daya Bay surface sediments is generally imperceptible. The metals’ potential risks to the environment were assessed, and the results showed that they have generally no risk or low risk except for Cd, Mn and Sr. 相似文献
14.
Total dissolvable metals (Co, Ni, Cu, Cd, and Pb) in both surface waters and the water columns were acquired in the southern East/Japan Sea during a cruise around the Ulleung Basin in June 2001 to understand the spatial distributions of the metals. Concentrations in offshore surface waters were found to be Co 60 ± 12 pM, Ni 2.16 ± 0.25 nM, Cu 1.85 ± 0.55 nM, Cd 0.134 ± 0.018 nM, and Pb 155 ± 40 pM. Spatial distributions in surface waters showed that metal levels were generally enhanced at coastal sites in both Korea and Japan, where the metal distributions indicated complex patterns due to inputs, biogeochemical processes, and physical factors including upwelling. The Co distributions in the water columns seemed to be influenced predominantly by surface and bottom inputs, scavenged rather than regenerated at depth. For Cd, there was generally good agreement between the Cd and PO4 depth distributions, in agreement with the literature. The Cd/PO4 ratio from the water columns was found to be 0.133–0.203, lower than that in other marginal seas (e.g. the East/South China Seas and the Philippine Sea) of the western Pacific Ocean; this might be a result of the fast ventilation rate in this sea. The vertical Pb profile showed typical scavenged-type behavior with a surface maximum and deep minimum. From a comparison of inputs from the atmosphere and the Tsushima Warm Current, atmospheric deposition is substantial enough that it cannot be ignored, and its role in metal cycling is more significant in the offshore zone. 相似文献
15.
The determination of Fe, Mn, Ni, Pb, Cu, Co, Zn, Cd, K and Na was carried out in the mesozooplankton caught in the southern Baltic in July 1980. The species structure of mesozooplankton was characterized on the basis of mean numbers of particular components and their percentage. The chemical analyses of the samples of mesozooplankton show a wide range of values, although they were within the ranges published for zooplankton from other aquatic regions of the world. Both concentration factors and selectivity factors for Zn, Cd, Pb and Cu in the organisms analysed were calculated. The significant cross-correlation coefficients calculated for all possible pairs of metals showed the following associations: CuPbNiMnFe, MnZn and NaZn. 相似文献
16.
The release and removal behaviour of Cd, Cu, Co, Ni, Pb and Zn from the sediment of Xiamen Harbour to sea water have been studied under ultra-clean laboratory condition within 168 b. Initial rapid increases in dissolved Cu, Pb, Zn and Co were observed in the first six hours and twelve hours respectively after addition of various amounts of sediment. Then Pb and Co decreased to background values, while Zn decreased to less than the background value and Cu remained unchanged. Cd and Ni did not increase during the experiment. The results indicated that the weakly bound heavy metals were released from the sediment through desorption or exchange. Simultaneously, they might form complexes or be adsorbed in colloids or particles. The two processes existed simultaneously, changing with time and conditions. 相似文献
17.
Abigail Parcasio Cid Syouhei Urushihara Tomoharu Minami Kazuhiro Norisuye Yoshiki Sohrin 《Journal of Oceanography》2011,67(6):747-764
The distribution of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb in seawater was investigated on the Bering Sea shelf (56–64°N,
165–169°W) in September 2000. The unfiltered and filtered seawater samples were used for determination of total dissolvable
(TD) and dissolved (D) metals (M), respectively. The TD-M concentrations were generally higher than in the Pacific Ocean.
TD-Cd was highest in deep water of the outer shelf domain and dominated by dissolved species. The other TD-M were highest
at stations close to the Yukon River delta and had higher fractions of labile particulate (LP) species that were obtained
as the difference between TD-M and D-M. Dissolved Al, Ni, and Cu were characterized by input from the Yukon River. Dissolved
Mn and Co showed maximums on the bottom of the coastal domain, suggesting influence of sedimentary Mn reduction. The correlations
of D-Zn, D-Cd, and macronutrients indicated their distributions were largely controlled through uptake by microorganisms and
remineralization from settling particles. All these three processes (river input, sedimentary reduction, and biogeochemical
cycle) had an influence on the distribution of D-Fe. D-Pb was fairly uniformly distributed in the study area. The stoichiometry
of D-M in the Bering Sea shelf showed enrichment of Co and Pb and depletion of Ni, Cu, Zn, and Cd compared with that in the
North Pacific. The LP-M/LP-Al ratio revealed significant enrichment of the other eight metals relative to their crustal abundance,
suggesting importance of formation of Fe–Mn oxides and adsorption of trace metals on the oxides. 相似文献
18.
海水养殖池沉积物中重金属形态和生物酶活性的关系研究 总被引：1，自引：0，他引：1
以连云港市对虾养殖池表层沉积物为研究对象,采用Tessier连续萃取法,研究了表层沉积物中重金属(Cu、Zn、Pb、Cd、Cr、As、Mn)的赋存形态和酶(脲酶、碱性磷酸酶、过氧化氢酶、转化酶)活性的相关性。结果表明,重金属Cu和Zn以有机-硫化物结合态为主要的赋存形态,Pb以铁锰氧化物态为主要的赋存形态,Cd以可交换态(平均33.47%)和碳酸盐结合态(平均31.16%)为主要存在形态,Cr和As主要以残渣态存在,Mn的铁锰氧化物态比例最高。脲酶的活性范围为0.45—8.96mg/(g·24h),碱性磷酸酶活性范围为2.45—6.69mg/(g·24h),过氧化氢酶活性范围为0.14—2.36m L/(g·min),转化酶活性范围为0.45—10.45mg/(g·24h)。脲酶活性与Cd、As的可交换态、Cd的碳酸盐结合态、Cu、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态之间显著相关;碱性磷酸酶活性与Zn、Cd的铁锰氧化物态显著相关;过氧化氢酶活性与Cd的可交换态、碳酸盐结合态及残渣态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫结合态之间显著相关;转化酶活性与Cu、Cd、As的可交换态、Cd的碳酸盐结合态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态、Cd、As的残渣态之间显著相关。酶活性可以用来指示海水养殖池沉积物中重金属的形态转化过程。 相似文献
19.
三亚湾滨珊瑚骨骼重金属与环境因子的关系 总被引：3，自引：0，他引：3
利用ICP-AES分析测定了南海北部三亚湾滨珊瑚(Porites)骨骼生长带1977—1999年问重金属Cr、Zn、Cd、Cu、Ph、Ni、V的含量。通过对重金属元素的因子分析，划分出2类元素组合：Zn、Cd、Cu、Ph、Ni组合和Cr、V组合。2类重金属元素组合与不同季节表层海水温度、降水量以及冬、夏季风指数等相关环境因子的逐步回归分析反映出具不同的重金属元素有不同的环境影响因子，其中Zn、Cd、Cu、Ph、Ni组合主要受春季表层海水温度的影响．Cr、V组合主要受冬季风强弱变化的影响。 相似文献
20.
In different samples of Mytilus galloprovincialis Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb and Zn were determined by AAS. The mussels were taken from 11 sites in the Port of La Spezia. Typical concentration ranges (μ/g dry weight) were as follows: Cd, 2.0–6.8; Co, 0.8–3.2; Cr, 5.8–19.5; Cu, 6.9–33.7; Hg, 0.15–0.38; Mn, 11.8–37.8; Ni, 1.3–10.9; Pb, 13.9–44.6 and Zn, 203–379.Other samples were collected at 4 sites on the Promontory of Portofino and the following values were obtained: Cd, 0.8–1.1; Co, 2.6–2.9; Cu, 3.3–4.2; Hg, 0.09–0.15; Mn, 6.3–9.1; Ni, 1.2–2.4; Zn, 120–140. 相似文献