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1.
选择了东太平洋赤道附近的系列成岩型铁锰结核(壳)样品,根据其中的矿物相的种类,利用化学上的相分析手段——选择性提取实验,借助晶体化学和矿物学手段对过渡金属元素Cu、Co、Ni、Ti和碱土金属元素Mg在成岩型铁锰结核中的地球化学特征进行了研究。结果显示,元素Cu、Co、Ni、Ti和Mg等元素在成岩型铁锰结核中的富集受这些元素在海水中的存在状态和结核中组成矿物这两方面因素的制约。成岩型结核中10-水锰矿结构的稳定性并不完全是由于其充分吸收了Cu、Co、Ni等过渡金属元素,碱土金属Mg对于10-水锰矿结构的稳定性起到了重要作用。 相似文献
2.
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
3.
不同成因的海洋铁锰氧化物沉积物中稀土元素的地球化学特征 总被引：1，自引：0，他引：1
测试了具代表性的成岩型结核和水成型结壳的稀土元素,以研究稀土元素在这两种成因的海洋铁锰氧化物沉积物的特征及其与成因的关系。稀土元素特征表明稀土元素没有参与成岩型结核的成岩作用。即没有加入到1nm水锰矿中去,而是加入到无定形铁的氧化物、氢氧化物中去。同样,稀土元素也没有直接参与水成结壳的水成作用,即没有加入到锰、铁的氧化物、氢氧化物中去,而是与钙、磷相关。推测在很大程度上是先沉淀在钙、磷相中然后才加入到水成结壳中。稀土元素在这两种类型的沉积物的分布与其成因密切相关。 相似文献
4.
本文通过对秘鲁海盆DEA区浅层埋藏型铁锰结核开展地球化学和矿物学研究,探讨了埋藏型大洋锰结核的有用组分的富集、清扫机制及成因类型。该区铁锰结核致密层和疏松层互层具有明显的多孔树状微结构,结核主要由10?锰矿相、7?锰矿相(水钠锰矿)和δ-MnO2(水羟锰矿)等锰相矿物组成,成分上具有高Mn、低Fe和中等Ni+Cu、Mo(分别为44.79%、0.55%、0.46%、0.05%)的亚氧化成岩型特征和低的Co、Ti、Zn和REY元素(REYSN均小于1)含量。铁锰结核中低含量的Mo和大部分的Ni与Mn氧化物清扫有关,其中Mo与Mn相关系数R=0.65,高Mn/Fe(>300)中Ni含量同样很高(0.34%),其他元素如Cu、Ti和REY均与Fe的羟基氧化物及铝硅酸盐相关性较高(R>0.8)。铁锰结核Fe、Ni+Cu、Mo、REY元素含量和Mn/Fe比值在分层上呈现规律性变化,致密层的CeSN负异常和疏松层的CeSN正异常进一步表明,铁锰结核的生长过程经历亚氧化-氧化成岩作用的环境条件变化,该变... 相似文献
5.
南海铁锰结核(壳)的元素地球化学研究 总被引：1，自引：0，他引：1
本文利用南海11个铁锰结核(壳)样品的化学分析资料,研究了铁锰结核(壳)中Fe,Mn,Cu,Co,Ni,Pb,Zn,Cr,K,Na,Ca,Mg,Si,P,Al,Ti,Sr,Ba及∑REE的元素地球化学特征。结果表明:(1)铁锰结核(壳)以高Fe,∑REE,低Mn,Cu,Co,Ni等元素为主要特征;(2)铁锰结核(壳)中Fe,Mn间无明显相关,而Fe与∑REE,∑Ce,∑Y呈弱的正相关,Mn与∑REE,∑Ce,∑Y呈明显的正相关,结壳中Fe,Mn与Si,Al,Cu Co Ni呈负相关;(3)结核(壳)中Mn/Fe与Cu/Ni,Ce/La呈负相关,Mn/Fe主要受Mn控制;(4)结核(壳)中Fe,∑REE等元素主要来自南海陆源中酸性岩类的风化、淋滤和沉积。 相似文献
6.
《热带海洋学报》2017,(2)
为了解南海北部不同海域铁锰结核中常微量、稀土元素的赋存特点及其富集机制,采用化学淋滤法提取南海北部上陆坡、下陆坡、深海盆3个区域铁锰结核的碳酸盐相、铁锰氧化相、残渣相组分,测定了常微量元素、稀土元素含量,揭示了不同相的元素赋存状态及其意义。Fe-Mn-(Cu+Co+Ni)判别图表明,上陆坡铁锰结核属于与冷泉流体相关的水成成因类型;下陆坡区和深海盆的铁锰结核形成环境相似,属于典型的水成成因类型。结核中K、Ca、Na、Mg、Sr主要富集在碳酸盐相,Fe、Mn、Ni、Cu、Zn、Pb主要赋存在铁锰氧化物相,Al、Ti和Mo主要出现在残渣相。常微量元素赋存状态变化受多种因素影响,钙质生物生产力的强弱和钙质生物碎屑的稀释作用是影响铁锰结核中碳酸盐相态元素变化的重要原因。铁锰结核的稀土元素主要富集在铁锰氧化物相,其次在碳酸盐相,而在残渣相的相对含量极少。不同海区铁锰结核稀土元素进入碳酸盐相的成因和机制基本相似,下陆坡和深海盆铁锰结核残渣相稀土元素配分模式相似,而与上陆坡铁锰结核的明显不同,残渣物质的来源、结核生长环境的氧化还原状态差异是主要影响因素。研究成果可为深入研究铁锰结核的元素迁移与转化、成矿作用与成矿物质来源及其相关的沉积环境、资源潜力评价等提供重要的基础资料。 相似文献
7.
菲律宾海的锰结壳和锰结核 总被引：3，自引：1，他引：3
西马里亚纳海盆和菲律宾海盆发育的锰结核是典型的深海结核。其丰度为0～15kg/m2,平均为3.5kg/m2,Ni+Cu+Co的平均含量为0.59%,最大含量为0.93%,平均Mn/Fe值为0.73.九州帛琉海脊和中央海脊发育的锰结壳和锰结核十分丰富。采集到的大块结壳表面直径可达到300～500mm,最大厚度为32～35mm,采集到的结核最大丰度可达到18.7kg/m2,Ni+Cu+Co的平均含量为0.62%,Co的含量最大为0.57%,平均Mn/Fe值为0.95.上述海盆和海脊上的结核和结壳主要锰矿物相均为水羟锰矿,属水成成因和较低的氧化生成条件,结核的形成时代为更新世以来。据结核和结壳的金属品位,尤其是Co的含量来看,目前尚不具经济潜力。 相似文献
8.
深海矿物沉积物,如铁锰结核和结壳,热液沉积物等,由于具有较高的经济潜力（尤其是出现于Ｃ—Ｃ区的铁锰结核）人们对其进行了最广泛的研究。Ｃ—Ｃ区中的成岩铁锰结核与水成结核相比富集１０Ａ°－水锰矿、Ｃｕ和Ｎｉ。然而,Ｃ—Ｃ区沉积物的孔隙水中富含溶解氧（有数十个μＭ）,其氧化还原条件不适合于过渡金属的再活化作用。ＫｌｉｎＲｈａｍｍｅｒ等（１９８２）断定中赤道太平洋的成岩铁锰结核中的Ｍｎ不是通过孔隙水向上扩散来供给的。Ｇｒａｙｂｅａｌ和Ｈｅａｔｈ（１９８４）根据沉积物的淋滤顺序,也报道了在目前的充氧深海… 相似文献
9.
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%~0.54%、0.08%~0.31%和0.01%~0.03%),主要由铁的羟基氧化物吸附的Ti,以及还会与钙磷酸盐发生耦合置换反应的REY的含量较高(分别为0.45%~1.88%、0.04%~0.19%),含量中等的Co(0.06%~0.27%)在铁锰相物质和硅酸盐相内核中分散分布。样品REY的标准化配分模式显示出明显一致的Ce正异常和Y负异常。铁锰结核从海水中捕获的Ce^3+容易被氧化成难溶且不具有活性的Ce^4+,Y则在结核内存在形式不稳定,容易发生解吸,致使Ce和Y分别呈现出相对于其他REY逐步富集和亏损的特征。研究区形成时间较晚,铁锰结核生长发育的时间不足,且四周地形较高,缺乏与外界连通的水道,阻碍了诸如来自南极的富氧底层流的大规模进入。区域内结核样品主要为水成型,成岩成因组分的供给太低,降低了主要有用组分的含量。以上诸多因素可能会导致区域内的铁锰结核难以富集成矿。 相似文献
10.
西太平洋深海盆地同时发育多金属结核和富稀土沉积物,但针对多金属结核及其表层沉积物之间关系的研究较少。通过多金属结核-表层沉积物地球化学分析,揭示关键金属元素在结核、沉积物中的富集和分馏过程,探讨沉积过程与环境对多金属结核生长的影响。研究区多金属结核具有相对高的Co、REY含量,低的Mn/Fe比值,显示为典型的水成成因。主成分分析及相关性分析结果指示结核的成矿过程是在水成作用、成岩作用以及陆地碎屑、生物碎屑输入的作用下,Fe-Mn氧化物对海水及孔隙水中各类金属元素的选择性富集。研究区表层沉积物主要为深海黏土,相较于多金属结核富集大部分金属元素,深海黏土更为富集Si、Al、Na、K等元素。沉积物中Co、Ni、Cu等金属元素的富集与Fe-Mn微结核的含量相关,而REY与磷酸盐组分更为密切。Fe-Mn氧化物组分对海水中金属元素选择性吸附形成多元素的富集及显著的Ce正异常、Y负异常,而磷酸盐组分主要继承海水的稀土特征,它们的含量决定了沉积物中金属元素及稀土元素的含量和模式。结核及沉积物在关键元素富集的过程中有相似的过程,Fe-Mn氧化物组分是二者元素富集过程的载体。研究区的低生物生产力和低沉积速... 相似文献
11.
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
12.
A widespread distribution of hydrothermal and hydrogenetic manganese deposits is described in the results of the Hakurei‐Maru cruises conducted in the Bonin Arc areas of the West Pacific from 1984 to 1989. Manganese deposits occur in the active volcano chains, back‐arc basins, remnant back‐arc ridges, and oceanic seamounts. The hydrogenetic iron‐manganese deposits commonly form earthly black crusts and nodules on the topographic highs of inactive ridges and old seamounts, sometimes as thick as 10 cm. They are always composed of the iron‐manganese mineral vernadite. Co and Ni contents are relatively high in the crusts from the seamounts in the open Pacific Ocean (up to 1.1% Co and 1.0% Ni). Two generations of distinct chemistry and texture are typical of these crusts, which can be compared to reported thick crusts from the Central Pacific seamounts. The hydrothermal deposits, characterized by dense, submetallic, and gray appearance, are dominant in the recent and also in past submarine volcanoes of the island‐arc systems. Evidence of past hydrothermal activity was ascertained as fossil hydrothermal manganese deposits inside the hydrogenetic nodules or beneath the hydrogenetic crusts over the Tertiary island arc. Their component minerals are considered to be todorokite and bimessite (stable and contractible upon dehydration), having almost negligible amounts of Fe, Si, Al, Ni, Co, Zn, Pb, Cu, etc. In the small model site, the Kaikata Seamount hydrothermal area, the presumably recent hydrothermal activity has yielded thin slabs of pure manganate deposits growing downward within volcanic and sand layers. Early diagenetic influence is negligible on nodules of this area. 相似文献
13.
The contents of Mn, Fe, Cu, Co, Ni, Pb and Zn in manganese nodules and associated pelagic sediment from the Northern Central Pacific have been measured, and the correlations between the elements of the nodules and between the chemical composition and the sedimentary environments have been analyzed. It has been found that Cu, Ni and Zn are preferentially enriched in the Mn-oxide phases while Co and Pb in the Fe-oxide phases of the nodules. The elements within the same phase are positively correlated and the elements within different phases are negatively correlated. It is concluded that the elements in the Fe-oxide phase may have directly deposited from seawater while Mn-oxide phase elements are mainly derived from interstitial waters. 相似文献
14.
为探究大洋富钴结壳的元素地球化学特征和赋存状态,以西太平洋麦哲伦海山群5个富钴结壳样品为研究对象,通过X射线衍射法、等离子体发射光谱法、等离子体质谱法及相态分析手段,分析了富钴结壳的矿物组成、主量元素和稀土元素含量。结果表明,富钴结壳样品主要结晶矿物为水羟锰矿,次要矿物包括石英、斜长石和钾长石,同时含有大量非晶态铁氧/氢氧化物。富钴结壳样品中Mn和Fe含量最高, Mn为16.87%～26.55%, Fe为14.34%～18.08%。富钴结壳明显富集稀土元素,其稀土总量为1 287～2 000μg/g,Ce含量为632～946μg/g,约占稀土总量的50%;轻稀土含量为1 037～1 604μg/g,重稀土含量为249～395μg/g,轻稀土元素明显高于重稀土元素。稀土元素配分模式呈现Ce正异常而Eu无异常,具有Ce富集特征。麦哲伦海山群富钴结壳是水成沉积成因,基本没有受到海底热液活动和成岩作用的影响。元素赋存状态与其矿物相密切相关, Na、K、Ca、Mg和Sr主要赋存于碳酸盐相, Mn、Ba、Co和Ni主要赋存于锰氧化物相, Fe、Al、P、Ti、Cu、Pb、V、Zn、Zr和REE主要... 相似文献
15.
Philomène A. Verlaan Author Vitae David S. Cronan Author Vitae Charles L. Morgan Author Vitae 《Progress in Oceanography》2004,63(3):125-158
Regional variation of Mn, Fe, Co, Ni and Cu in ferromanganese oxides (nodules and crusts) in the central south Pacific is related to primary productivity, oxygen minimum layer, and calcium carbonate compensation depth. The largely latitudinal influence of these environmental parameters on nodule and crust composition reflects their predominantly latitudinal variation. Primary productivity is the principal regional environmental control, influencing diagenetic enrichment of these elements in nodules through its effect, mediated by the CCD, on supply and concentration of labile organic matter vs. carbonate remains to the sediments. It influences hydrogenetic enrichment of these elements in nodules and crusts through its effect, mediated by the oxygen minimum layer (mainly in the case of crusts), on their export from surface waters.The elements’ varying susceptibility to being scavenged or organically bound influences the contrasting composition of diagenetic vs. hydrogenetic ferromanganese oxides, which is further influenced by depth. Hydrogenesis is the fundamental process governing nodule and crust formation, superimposed on which is diagenesis under specific circumstances; both are subject to intermittent interruption, diminution and augmentation by changes in environmental parameters. Application of regionally operative environmental controls locally explains local compositional variations and helps refine exploration criteria for economically viable nodules and crusts. 相似文献
16.
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
17.
In the Central Indian Basin manganese nodule abundance was variable in all sediment types. Mean abundance varied from 1.5 in calcareous ooze to 10.2 kg/m2 in terrigenous-siliceous ooze sediments. Nodule grade and growth rates are positively correlated only up to 10 mm/My (million years), and grade shows no distinct relationship with abundance. Relationships between the morphochemical characteristics of the nodules and host sediment types are subtle. Both hydrogenetic and diagenetic nodules (with smooth and rough surfaces respectively) occur on almost all sediments, but in variable proportions. Thus, the overall distribution pattern shows that small nodules (<4-cm diameters) of lower grade (average value Ni+Cu+Co=1.21%) with smooth surfaces are more common on red clay, terrigenous, and terrigenous-siliceous ooze transition-zone sediments. By contrast, large nodules (>4-cm diameters) of higher grade (average value Ni+Cu+Co=1.80%) with rough surfaces are more prevalent on siliceous ooze, siliceous ooze-red clay, and calcareous ooze-red clay transition-zone sediments. This implies an enhanced supply of trace metals from pore waters to rough-surface nodules during early diagenesis. 相似文献
18.
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
19.
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