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1.
Noburu Takematsu 《Journal of Oceanography》1979,35(1):36-42
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.
Noburu Takematsu 《Journal of Oceanography》1979,35(5):191-198
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
3.
The behavior of transition metals (Co, Ni, Cu and Zn) on precipitation of manganese oxides from seawater pumped up from a
well at the site of the Marine Science Museum, Tokai University, and collected from several tanks along the water supply system
to an aquarium was investigated. The distribution coefficients of cobalt and nickel between manganese oxides and seawater
were different at different sampling points along the water supply system. At sampling points with high rates of manganese
oxide precipitation, the distribution coefficients were about one order of magnitude smaller than those at the points with
low precipitation rates, while there were no remarkable differences in the distribution coefficients of copper and zinc among
the sampling points. The distribution coefficients of minor transition metals, with the exception of copper, observed at the
points with low precipitation rates were comparable to those measured experimentally using manganese dioxides. 相似文献
4.
借助相分析中的偏提取方法对取自东太平洋深海平原上的成岩型铁锰结核进行了选择性提取实验以研究稀土元素在其中各矿物或氧化物相中的分布模式以及铁氧化物和锰氧化物对稀土元素的吸附机制.结果显示,尽管1 nm-水锰矿相对无定形铁的氧化物/氢氧化物而言是成岩型结核中的优势矿物,但是稀土元素主要富集在无定形铁的氧化物/氢氧化物中.虽然稀土元素在海水中主要是以碳酸盐络合物的形式存在,但是无定形铁的氧化物/氢氧化物则是从海水中获得自由稀土元素离子来络合,而1 nm-水锰矿则直接吸附稀土元素的碳酸盐络合物.因此,无定形铁的氧化物/氢氧化物对稀土元素来说具有比1 nm-水锰矿更强的络合能力.成岩型结核的Ce负异常是由于成岩型结核形成于缺氧微环境中,该环境不能把可溶性的Ce~(3+)氧化成不溶性的Ce~(4+)发生沉淀. 相似文献
5.
对海水中锰的光化学反应及其影响因素进行了研究.实验结果表明,锰的光化学反应主要通过有机物为媒介进行,反应液中加入的有机物种类和浓度的改变会导致锰的光化学反应速率的改变.增加光强,有利于锰的光还原反应的进行.降低体系的pH值,可提高锰的光反应速率.锰在不同介质中光反应速率从大到小的顺序为:去离子水、人工海水、天然海水.此外,搅拌有利于锰的光反应的进行,但在体系分布已达均匀的前提下,搅拌速率的大小对锰的光反应速率几乎无影响.研究表明,通过光化学反应,海水中的锰会由四价的颗粒态转化为二价的可溶态,从而有利于浮游植物的吸收和生长. 相似文献
6.
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
7.
G.P. Glasby 《Marine Chemistry》1973,1(2):105-125
The rare-earth distribution has been determined in five manganese nodules from a range of marine environments. Manganese nodules from Loch Fyne, Scotland, and the Gulf of Aden are characterized by a low absolute abundance of the rare-earth elements and a low Ce/La ratio compared with deep-sea nodules. This difference is interpreted in terms of the diagenetic remobilization of manganese in the high sedimentation regimes leading to the effective fractionation of manganese from the rare-earth elements and the resultant depletion of the rare earths in nodules from these environments. The mechanism of incorporation of the rare-earth elements into manganese nodules is thought to be either the direct adsorption of these elements from seawater or the scavenging of the elements by colloidal iron oxide prior to their incorporation into the authigenic phase of nodules. There appears to be no evidence for the surface transfer of these elements from inorganic detritus into the authigenic phase of nodules as suggested by previous authors. The distribution of U and Th in the nodules is controlled by factors similar to those controlling the rare-earth abundance in nodules. The higher U/Th ratios in nodules from Loch Fyne and the Gulf of Aden is considered to be due to the preferential reduction of UO2(CO3)34? to some lower-valency uranium species such as U3O8 in nodules from less oxidizing environments. 相似文献
8.
Selective chemical attack has been used to separate recent surface marine sediments into organic, non-detrital and detrital components, and the concentrations of iron, manganese, copper and zinc in each fraction determined. The non-detrital fraction controlled the overall elemental concentrations and relationships apparent in the bulk sediment, particularly in the cases of copper, manganese and zinc. Copper was found associated with the organic fraction. The predominant processes of primary deposition are precipitation of hydrated ferric oxide and adsorption of copper and zinc onto this material. 相似文献
9.
Yoshio Sato 《Journal of Oceanography》1989,45(4):270-278
At the Minamichita Beach Land (Mihama-cho, Aichi, Japan), seawater is pumped up from underground and is supplied to aquaria. The underground seawater containsca. 2 ppm of Fe (II), 0.1 ppm of Mn (II) and a little dissolved oxygen. Iron oxide is formed in the seawater when aerated. The oxidation rate of Fe (II) was measured to be 1.4×1014 mol–3
l
3 min–1, which is comparable to the lowest values in the literature. The slow rate of Fe (II) oxidation obtained here can be attributed to the presence of organically bound iron in the seawater. The distribution coefficient of cations between seawater and iron oxide phase was in the order of Cu>Ni>Co>Cd>Mn, which is consistent with that predicted from their hydrolysis constants. The adsorption affinity sequence of oxyanions was phosphate >vanadate> molybdate. The difference in phosphate from the prediction of the adsorption theory was attributed to the formation of ferriphosphate on the oxide surface. On the basis of these data, the limitation and usefulness in the application of the distribution coefficients to marine environments were discussed. 相似文献
10.
The seawater chemistry of potentially toxic metals can affect their availability to marine organisms. Investigation of the relationship between metal chemistry and metal bioavailability has progressed slowly due to difficulties in controlling and measuring metal speciation in uptake media. Recent work with strong metal chelators such as NTA and EDTA has allowed a closer examination of how metal chemistry relates to biological accumulation and toxicity.1–3 However, the presence of a strong chelator at membrane transport sites and the possible alteration of microenvironments by strong chelators could create unnatural uptake behavior. This study presents another method for stabilizing metal chemistry in accumulation experiments. A cation exchange resin was used to study Mn54 accumulation by a small bivalve Donax variabilus. The resin proved an effective method for buffering manganese chemistry in seawater and could provide a useful tool to look for subtle effects present in other metal buffered seawater systems. 相似文献
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13.
海水利用是解决沿海地区淡水资源短缺的重要途径,但其排放的废水可能对海洋生态环境造成不利影响。文中分析了海水的盐度、温度以及携带的化学物质对海洋生态环境的潜在威胁,结果表明:浓海水、温排水排海可能会破坏排放海域的生态环境,影响海洋生物的繁殖、生长和发育,从而导致生物的种类数量、生物量和分布范围等发生变化,需要引起关注和重视。建议海水利用工程建设合理选址、优化设计,鼓励采用循环经济产业模式,延伸海水利用产业链条,以降低对海洋环境的不利影响;并加强排海废水对海洋生态环境影响的研究和监测工作,为改扩建或新建海水利用工程提供环境影响评价依据。 相似文献
14.
为促进我国海水淡化产业的可持续发展,文章分析海水淡化工程对环境的影响,重点分析浓海水对海洋生态环境的影响,并提出应对措施。研究结果表明:海水淡化工程在能耗、排污、用地、取水和噪音等方面对环境产生影响,尤其是海水淡化产生的浓海水,在温度、盐度、有机物和营养盐、重金属、酸度、余氯、溶解氧以及机械卷载效应等方面严重影响海洋生态环境和海洋生物,亟须高度关注和深入研究;随着我国海水淡化产能的增加,应完善海水淡化技术、优化浓海水排放和加快浓海水综合利用,同时健全相关法律法规和标准规范。 相似文献
15.
The stable form of dissolved chromium in oxygenated seawater is Cr(VI). But Cr(III)-species are also present at an analytically significant level. It is shown that Cr(III) is oxidized only slowly by dissolved oxygen, and that manganese oxide is a strong catalyst for such oxidation. However, the low oceanic concentration of suspended MnO2 impedes the conclusion that the former process is quantitatively less important than the latter one. The distribution of dissolved chromium among Cr(VI)- and Cr(III)-species is probably kinetically controlled. 相似文献
16.
良好的环境质量是厦门成为一个宜居和滨海旅游城市的重要基石。自日本福岛核事故发生和福建省核电站陆续运行之后,厦门邻近海域潜在的核污染风险受到公众和管理部门的关注。本研究测定了2015年2月和8月厦门邻近海域海水和海洋沉积物中主要放射性核素的含量水平,并据此评价了该海域的环境放射性质量状况。结果表明海水中总铀、90Sr、226Ra、137Cs处于我国海洋放射性水平变化范围以内,无明显季节差异,其他放射性核素58Co、60Co、134Cs、110mAg、59Fe、54Mn、65Zn均未检出,海水中90Sr和137Cs的活度最大值远低于国家海水水质标准限值,海洋沉积物中放射性核素活度水平亦在我国海洋放射性水平变化范围以内。利用我国现有的海洋放射性环境质量评价方法对厦门邻近海域放射性质量状况进行分级评价得出其海水放射性质量为2级,海洋沉积物放射性环境质量为1级,均属于安全级别。研究结果表明2015年在厦门附近海域未观测到放射性污染现象。 相似文献
17.
Michael S. Hutcheson 《Marine environmental research》1983,9(4):237-255
The acute lethality and sublethal heavy metal contamination potential to marine organisms of a waste brine solution from a potash mining operation were determined. The brine was acutely lethal to marine organisms of the Bay of Fundy, Canada, at concentrations between 47 and 55‰ salinity (96-h LC50 values: threespine stickleback, Gasterosteus aculeatus, 47·7‰; polychaete worm, Nephtys incisa, 52·5‰; blue mussel, Mytilus edulis, lethal to whole animal and reduced ciliary activity of gills above 55‰).The brine diluted to sublethal concentrations (≤40‰) contained manganese (≤ 49·5 ×), copper and zinc (≤ 5·2 ×), lead (≤ 2·6 ×) and cadmium (≤ 0·7 ×) in decreasing order of enrichment relative to control seawater. Copper was accumulated in mussels exposed to these solutions over 44 days to the greatest degree (4 ·4 ×), followed by manganese and lead. Tissue lead concentration reached a steady value within 44 days and cadmium was not accumulated. 相似文献
18.
A simple colorimetric method was developed for determining molybdenum in seawater by solvent extraction of its dithiolate and was then applied during a nine month study of Saanich Inlet. This inlet is a fjord on the coast of Vancouver Island, British Columbia, in which the bottom waters alternate between a weakly oxygenated and anoxic state. Results are given for the concentrations of dissolved and suspended molybdenum, suspended manganese, dissolved oxygen and of salinity measurements. Salinity-molybdenum correlations demonstrate that the deep waters are deficient in molybdenum, a conclusion consistent with reports that the sediments deposited in the reducing zone are enriched with molybdenum precipitated from the anoxic bottom waters. Suspended manganese, which occurs in large amounts as a result of the oxidative precipitation of dissolved Mn(II) diffusing from anoxic waters, has a distribution that is directly correlated to that of suspended molybdenum and which tends to be inversely related to that of dissolved molybdenum, suggesting that molybdenum is being coprecipitated with manganese oxides. Such a hypothesis is supported by the fact that the average molybdenum to manganese weight ratio of suspended matter closely approximates that of local manganese nodules, and by a mathematical analysis of the distribution data which includes development of a model for scavenging. Computations using the model relationships indicate that manganese oxide scavenging tends to concentrate molybdenum in the reducing waters where the anoxic processes responsible for its deposition in the sediments become operative. Additional calculations based upon current estimates of oceanic residence times suggest that manganese-oxide scavenging operating on an oceanic scale could be removing approximately 10% of the molybdenum being added to the oceans. 相似文献
19.
海洋浮游细菌生长率和被摄食的研究综述 总被引：2，自引：0，他引：2
海洋浮游细菌利用海水中的溶解有机碳合成自身物质,是海洋浮游生态系统的二次生产者。微型浮游动物是细菌的主要摄食者,也是细菌生产向较高营养级传递的中介。研究海洋浮游细菌的生长率和被(微型浮游动物的)摄食率对理解海洋浮游生态系统的功能具有重要作用。本文综述了利用改变海水中生物类群组成(或功能)的培养方法研究海洋浮游细菌生长率和被摄食率的历程和现状,为我国的同类研究提供借鉴。改变海水中生物类群组成(或功能)进行培养的方法有海水分粒级培养、海水稀释培养和添加选择性抑制剂培养。这些方法各有其局限性,应用并不广泛。细菌及其主要摄食者异养鞭毛虫群落在自然海区和实验室内都有生长周期,鞭毛虫的生长周期落后于细菌,因此细菌的生长率有时会小于被摄食率,有时会大于被摄食率。我国这方面的研究相对落后,应值得引起重视,建议从海水稀释培养法入手开展相关研究。 相似文献
20.
太平洋海山富钴结壳中铂族元素赋存状态与富集机理 总被引：2，自引：1，他引：1
通过选择性化学提取法,对太平洋采薇海山富钴结壳样品中铂族元素进行分级提取实验,利用电感耦合等离子体质谱仪(ICP-MS)测定了铂族元素含量。赋存状态结果显示,富钴结壳中铂族元素在各个化学相态中富集比例从大到小依次为:铁氧化物相、残渣态、锰氧化物相、碳酸盐相、吸附态,未磷酸盐化新壳层和磷酸盐化老壳层中铂族元素都主要赋存于铁氧化物相中,其富集比例为59.26%～82.19%,残渣态中磷酸盐对铂族元素具有一定的富集能力,其富集比例为17.23%～35.37%。不同类型地质体中铂族元素的赋存状态结果,也证实了富钴结壳和海山结核中铂族元素富集主要受到铁氧化物相和残渣态的影响。太平洋海山富钴结壳中铂族元素的富集机理推测为铁氧/氢氧化物胶体粒子的吸附作用,使海水中PtC l24-离子被吸附到铁氧化物相中,从而使富钴结壳中铂族元素富集。 相似文献