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1.
Experiments of sorption of Mn, Co, Ni, Cu and Zn on manganese oxides, hydrated ferric oxide, Na-montmorillonite and treated red clay are carried out in connection with the mechanisms by which transition metals are removed from seawater in marine environments.The order of sorption affinities of transition metals for Na-montmorillonite, treated red clay and hydrated ferric oxide is Mn相似文献   

2.
Produced water undergoes changes in its physical chemistry including precipitation of heavy metals after being discharged and mixed with ambient seawater. Potential impacts of the precipitation of heavy metals on their transport and toxicity were studied using samples from offshore oil production sites on the Scotian Shelf off eastern Canada. Concentrations of aluminum, cadmium, chromium, cobalt, copper, iron, lead, manganese, nickel and zinc were measured in total, particulate and dissolved fractions together with Microtox tests for assessment of toxicity. Heavy metals in produced water were transformed from dissolved to particulate phase in a period of hours under oxygenated conditions, and aggregated to larger particles that settle rapidly (>100 m/day) over a few days. In addition, there was production of buoyant particles comprised of heavy metal precipitates sequestered onto oil droplets that were transported to the surface. The particulate fraction was generally more toxic than the dissolved fraction. This was evident at the mixing interface between produced water and seawater where elevated particulate and toxicity levels were observed. Laboratory studies suggest an increase in the toxicity of discharged produced water over time. Time-series experiments showed a sustained toxic response for more than a week following the oxidation of freshly discharged produced water that initially elicited little or no toxic response in the Microtox test. Chemical processes identified in this study, namely precipitation of heavy metals and consequent settling and rising fluxes of particles, will influence the toxicity, the fate and the transport of potential contaminants in the produced water. Therefore, these processes need to be considered in assessment of the environmental impact associated with offshore oil and gas operations.  相似文献   

3.
Metal-organic complexes of transition elements removed by Amberlite XAD-2 resin from seawater pumped up from under the ground were determined. The proportions of iron, copper and zinc retained on the resin to dissolved forms of these metals were about 70, 40 and 5%, respectively, while manganese, cobalt and nickel were not retained on the resin. These results suggest that although iron may be retained in colloidal form, a significant fraction of copper is present in some organic form(s).  相似文献   

4.
This is the first article to describe mineralization of midplate submarine rift zones and hydrothermal manganese oxide mineralization of midplate volcanic edifices. Hydrothermal Mn oxides were recovered from submarine extensions of two Hawaiian rift zones, along Haleakala and Puna Ridges. These Mn oxides form two types of deposits, metallic stratiform layers in volcaniclastic rocks and cement for clastic rocks; both deposit types are composed of todorokite and bimessite. Thin Fe‐Mn crusts that coat some rocks formed by a combination of hydrogenetic and hydrothermal processes and are composed of δ‐MnO2. The stratiform layers have high Mn contents (mean 40%) and a large fractionation between Mn and Fe (Fe/Mn = 0.04). Unlike most other hydrothermal Mn oxide deposits, those from Hawaiian rift zones are enriched in the trace metals Zn, Co, Ba, Mo, Sr, V, and especially Ni (mean 0.16%). Metals are derived from three sources: mafic and ultramafic rocks leached by circulating hydrothermal fluids, clastic material (in Mn‐cemented sandstone), and seawater that mixed with the hydrothermal fluids. Mineralization on Haleakala Ridge occurred sometime during the past 200 to 400 ka, when the summit was at a water depth of more than 1,000 m. Hydrothermal circulation was probably driven by heat produced by intrusion of dikces, magma reservoirs, and flow of magma through axial and lateral conduits. The supply of seawater to ridge interiors must be extensive because of their high porosity and permeability. Precipitation of Mn oxide below the seafloor is indicated by its occurrence as cement, growth textures that show mineralizing fluids were introduced from below, and pervasive replacement of original matrix of clastic rocks.  相似文献   

5.
Mobilization and transfer of atmospherically transported metals to major suspended particulate matter components in seawater have been studied in a multichamber leaching experiment. Data on the meteorological air mass history, enrichment factors and sequential extraction analysis indicate that the highly polluted marine aerosol samples collected on Helgoland are of anthropogenic origin. A significant fraction of the total cadmium (81%), zinc (58%), copper (41%), and lead (40%) was released in seawater within 1 h. When exposed to the aerosol and artificial suspended particulate matter components for another 100 h, a portion of the released metals ranging from 10 to 60% was readsorbed. Zinc and lead were scavenged by iron/manganese oxides or readsorbed by the aerosol particulates. Of the total scavenged copper portion 67% was bound to phytoplankton cell walls which evidences an ecological impact of the polluted marine aerosols even in the coastal environment.  相似文献   

6.
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   

7.
东海泥质区表层沉积物中铜和铅的赋存形态研究   总被引：1，自引：0，他引：1  
2007年11月在东海泥质区13个站点采集了表层沉积物样品,用连续提取法分离并测定了铜和铅的赋存形态。结果表明,铜主要赋存于易还原态(铁锰氧化物结合态),含量为1.2～5.1μg/g,平均值为3.3μg/g;铅主要赋存于碳酸盐结合态,含量为1.9～7.3μg/g,平均值为5.3μg/g。泥质区铜和铅的有机结合态和易还原铁锰氧化物结合态与水深之间的呈明显的相关关系,碳酸盐结合态则与水深不相关。铜和铅非残渣态总量与采样站点水深之间的关系受控于其主要赋存形态,反映了重金属形态分布受到陆源输入和在水体中迁移等因素的影响。济州岛西南泥质区表层沉积物中铁锰氧化物结合态的铜和铅含量高于其他海区表层沉积物,可能是由于沉积物再悬浮所致。  相似文献   

8.
To study biological effects on the particulate removal of chemical elements from seawater, sediment trap experiments were carried out successively ten times throughout the spring phytoplankton bloom in Funka Bay. Sediment traps were deployed every one to two weeks at 1, 40 and 80 m depths. The settling particles obtained were analyzed for trace metals, phosphate and silicate. The propagation of diatoms in spring results in larger particulate fluxes than that of dinoflagellates. The biogenic silicate concentration is higher in the earlier period, when diatoms are predominant, than in the subsequent period, when dinoflagellates are predominant. The concentrations of aluminum, iron, manganese and cobalt in the settling particles comprising largely biogenic particles are lower during phytoplankton bloom. The concentration of copper is not reduced by the addition of biogenic particles, and its vertical flux is approximately proportional to the total flux, indicating that its concentration in the biogenic particles is nearly equal to that in the non-biogenic particles. The results for nickel and lead show the same tendency as for copper. Cadmium is more concentrated in biogenic particles than in non-biogenic particles, and the concentration of cadmium in the settling particles decreases with depth, similarly to phosphate and organic matter. Thus, metals in seawater are segregated by biological affinities, and the degree of incorporation into biogenic particles is in the order Cd > Pb, Ni, Cu > Co > Mn, Fe, Al. Biogenic particles are the most important agent controlling the vertical distribution of metals in the ocean. They remove the metals from the surface water, transport them through the water column, and regenerate them in the deep.  相似文献   

9.
The contents of oxyanionic elements (V, Se and Mo) and cationic transition metals (Mn, Fe, Co, Ni, Cu and Zn) in sediments from near-shore to deep-sea environments were measured to clarify factors regulating the distribution of these elements in marine sediments. For cationic transition metals of which contents increase from near-shore to deep-sea environments, the chemical composition of pelagic clays is modeled by a mixture of aluminosilicates having the chemical composition of average shale and Fe–Mn oxides having the chemical composition of associated manganese nodules. The content of V is fairly constant in sediments from near-shore to deep-sea areas. The mixture model of average shale and manganese nodules holds also for V, although most of the V is located in the aluminosilicate lattices. The content of Se in the near-shore sediments is higher and that in the deep-sea sediments is lower than that in average shale. The high content in the near-shore sediments is interpreted as the addition of biogenic materials to aluminosilicates with average shale composition and the low content in deep-sea sediments is explained by oxidative release of Se from aluminosilicates. The content of Mo in sediments increases from near-shore to deep-sea environments. The general distribution of Mo in marine sediments is expressed by the mixture model. An anomalously high content of Mo in a near-shore sediment is attributed to adsorption of molybdate on manganese oxides.  相似文献   

10.
Experiments on the uptake of Zn and Cd by synthetic hydrous Mn oxides were carried out in an ionic medium at pH 3.5 and at pH 4. A slight preference for uptake of Cd2+ over Zn2+ was observed with both birnessite and nsutite, the Cd/Zn ratio being different for each mineral. Subsequently, the desorption of Zn and Cd from the obtained products in artificial seawater was studied. In this medium Cd is desorbed from the Mn oxides to a much higher extent than is Zn. The latter observations can be satisfactorily explained by the large difference of complex formation for the two metals in seawater, slightly counteracted by the preferential uptake of Cd2+ over Zn2+. The order of magnitude of the Zn/Cd ratio in natural manganese nodules is compatible with the ratio calculated on the basis of experimental results, taking fair estimates of the actual inorganic Zn/Cd ratio in seawater and of the pH of deep ocean water.  相似文献   

11.
Abstract. During the austral summer 1997–98, within the framework of the activities of the Climatic Long-term Interaction for the Massbalance in Antarctica (CLIMA) Project of the Italian National Program for Antarctic Research (PNRA) in the Ross Sea, measurements were conducted to focus on the role of dissolved iron, copper and manganese as micronutrients, and on their distribution in suspended particulate matter in different water masses. Sampling was carried out in two selected shelf areas, both important for formation and mixing processes of the water bodies.
Metal data were evaluated together with physical measurements and classical chemical parameters such as oxygen and nutrients.
In both the studied areas, the distribution of dissolved metals along the waste column confirmed their micronutrient behaviour, showing depletion where phytoplanktonic activities occurred.
The trend of particulate metals underlined the scavenging phenomena along the water column and presented an interesting correlation at intermediate depths with the amount and origin of suspended matter.  相似文献   

12.
Concentrations of dissolved iron, manganese, molybdenum, copper, and organic carbon (DOC) were measured in the pore waters from surficial sediments of a temperate estuary to delineate seasonal metal remobilization from 1978 through 1980. Iron and DOC data were collected for 31 months and covaried inversely and exponentially. Iron dissolution occurred during the spring and during periods of active bioturbation with concentrations as high as 18 mg 1?1. Iron values were low during winter due to oxidation to ferric oxides. The lack of active bioturbation during the summer of 1978 allowed for the nearly complete removal of iron as a monosulfide precipitate. However, bioturbation resumed during the summer of 1979 and 1980 and dissolved iron concentrations as high as 10 mg 1?1 were observed at those times. The iron and DOC data were a qualitative measure of bioturbation activity. Dissolved manganese, molybdenum, and copper data were collected for 18 months during 1978 and 1979. All three metals displayed spring maxima covariate with iron, suggesting that they behaved chemically like iron and/or were associated with iron- or manganese-rich phases during this time of the year. In general, manganese and molybdenum varied temporally with iron while copper concentrations mimicked iron variations only during the spring.  相似文献   

13.
The aim of this study is to understand the various sources and factors controlling the abundance and distribution of the metals through the analyses of selected metals (iron, manganese, chromium, copper, zinc and cobalt), sand, silt, clay, organic carbon and magnetic susceptibility of the surface sediments of Zuari estuary in three different seasons. Total suspended matter (TSM) concentration and salinity of near surface and bottom waters were also measured. The study undertaken for three seasons, based on 18 selected stations all along the estuary, indicated that the concentration of most of the metals were comparatively higher during pre-monsoon than in monsoon and post-monsoon seasons. Further, along the length of the estuary, high concentrations were observed at lower middle and lower estuary and also at few stations at the upstream end. Salinity, distribution of TSM, size of the sediment, organic matter, geomorphological setup, fresh water input from land and release of industrial waste within the estuary played a role in distribution and concentration of metals. Magnetic measurements indicated the dominance of haematite like minerals and helped in understanding the source and depositional processes.  相似文献   

14.
The mechanisms of incorporation of minor transition metals into marine manganese nodules are discussed on the basis of differential chemical leaching.A small portion of iron and manganese in deep-sea nodules was dissolved in dilute acetic acid. Hydrogenous cobalt and nickel in nodules were also slightly leached with the acid solution, while 50–60 % of hydrogenous copper and zinc were leached. This difference suggests that the greater parts of hydrogenous cobalt and nickel are present in the lattices of manganese oxide phases, while the major parts of hydrogenous copper and zinc are present in the sorption sites of manganese oxide phases.The enrichment of minor transition metals in manganese nodules may be controlled by their substitution for manganese atoms in manganese oxide lattices after their sorption on manganese oxide phases.  相似文献   

15.
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   

16.
Amberlite XAD-1 resin was examined to test its suitability for extracting organic complexes of copper, zinc and iron from seawater. At low flow rates and at loading capacities far below theoretical values, the adsorption of these metals is not reproducible and the results are reminiscent of the behaviour observed when the adsorption capacity is being exceeded or flow rates are too high. It is suggested that the resin also adsorbs small but significant amounts of inorganic ions from seawater and that this effect makes the resin unsuitable for quantitative measurements of trace metal speciation.  相似文献   

17.
深海铁锰结核能有效记录海域内重大地质事件和气候环境信息,且富含多种金属物质极具资源潜力,因而广受关注.通过对帕里西维拉海盆西侧边缘中段海域内新发现的12个站位铁锰结核的地球化学特征研究,发现与全球主要成矿区内的铁锰结核相比,Mn及主要赋存在锰氧化物中的Ni、Cu、Mo的含量较低(分别为8.20％～25.24％、0.11...  相似文献   

18.
We analyse the distribution of the dissolved forms of cadmium, lead, cobalt, copper, and manganese in the near-Danube part of the Black Sea and in a section made at 45° 10′N in the autumn of 1997. It is shown that the discharge of rivers results in the appearance of significant amounts of cadmium, lead, cobalt, copper, and manganese in the near-Danube region. Copper is the most labile element in this collection of metals. Its behaviour is correlated with the vital activity of diatomic algae. The distribution of dissolved manganese in the near-bottom region is correlated with the distribution of O2. Indeed, the elevated concentrations of manganese are observed in the regions with low concentrations of oxygen. Translated by Peter V. Malyshev and Dmitry V. Malyshev  相似文献   

19.
Specimens of Bathymodiolus azoricus were sampled along the Mid-Atlantic Ridge at the Menez Gwen, Lucky Strike and Rainbow hydrothermal fields. Individual shells (n = 51), through the weight range 0.62 to 15.70 g, were analyzed for their magnesium, strontium, iron, manganese, copper, zinc and cadmium concentrations. Amongst the marine molluscs the shell of B. azoricus is confirmed as being particularly impoverished in strontium (mean 943 microg g(-1)). Trace metal concentrations in the shells decreased in the order Fe> Mn> Zn> Cu> Cd. Despite originating from trace metal rich environments mean concentrations were low (37.9, 13.2, 10.7, 1.1 and 0.7 microg g(-1), respectively). Irrespective of geographical origin magnesium, strontium and copper concentrations were primarily dictated by shell weight. In contrast cadmium concentrations were elevated in shells from the Rainbow field and ambient seawater chemistry imparted site specific chemical fingerprints to the shells with respect to the iron to manganese ratio.  相似文献   

20.
Using a clean seawater sampling system for trace metals onboard the R. V. Shinsei-Maru, newly launched in 2013, we investigated the vertical distributions of dissolved iron and zinc in Sagami Bay and the Izu-Ogasawara Trench. We applied appropriate clean sampling and filtering processes for trace metals, so that uncontaminated seawater samples were successfully collected. The distribution of zinc in the trench area was similar to that of silicate and the same as that previously reported in the subtropical North Pacific. There were spatial variations in the iron (Fe) distribution in the trench areas. We used previously reported information about biogeochemical cycling in the trench area, and found that Fe has a residence time of 29 years in the water column. The short residence time of Fe (29 years) corresponds to the vertical variations of dissolved Fe in the water column.  相似文献   

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