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1.
太平洋铁锰结壳的锶同位素地球化学研究   总被引:5,自引:0,他引:5  
本文研究中太平洋的翰斯顿岛卡林海山铁锰结壳RD4-2和东太平洋海盆铁锰结壳5405的锶同位素组成特征,并利用铁锰结壳的锶同位素组成与大洋海水锶同位素演化标准曲线对比,推断出结壳生长起始年龄、接三元混合模式,计算玄武质组分和硅铝质组分对锶同位素的贡献。  相似文献   

2.
大洋富钴结壳成因机制的探讨——水成因证据   总被引:3,自引:0,他引:3  
根据对大洋富钴结壳的分层与年龄、分层与生长速率、生长间断等观测事实,以及大洋富钴结壳主量元素锰、铁元素及钴元素、铂元素、稀土元素、氦同位素、锇同位素等的水成富集,指出大洋富钴结壳是水成因的,进而指出富钴结壳的形成与基岩无关,水动力条件、最低含氧带、生物作用等可能对富钴结壳的形成有控制作用。同时,富钴结壳不一定只生长在岩石裸露的海山上,在沉积物覆盖的海山区也有可能找到富钴结壳。  相似文献   

3.
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   

4.
利用等离子体发射光谱法、等离子体质谱法以及相态分析手段,对太平洋徐福海山富钴结壳稀土和铂族元素地球化学特征、赋存状态及富集机制进行研究。结果表明,富钴结壳稀土和铂族元素明显富集,其稀土总量为1 842~2 854 μg/g,铂族总量为144~1 180 ng/g,老壳层中稀土和铂族元素含量明显高于新壳层,这可能与老壳层发生磷酸盐化作用有关。轻稀土元素含量明显高于重稀土元素含量,呈现Ce正异常而Eu无异常,具有明显Ce富集特征。铂族元素之间发生了明显分异作用,PPGE含量明显高于IPGE,表现出明显Pt正异常而Pd负异常,具有明显Pt富集而Pd亏损特征。稀土元素赋存状态显示,新壳层中稀土元素主要赋存于铁氧化物相,其富集比例为65.40%~70.05%,老壳层中稀土元素主要赋存于残渣态,富集比例为62.27%~65.77%,这可能与残渣态中磷酸盐有关。铂族元素赋存状态显示,新壳层和老壳层中铂族元素都主要赋存于铁氧化物相,其富集比例为63.66%~69.51%,残渣态(29.20%~34.68%)对铂族元素也有一定的富集能力。富钴结壳稀土和铂族元素的富集推测为铁氧化物胶体粒子的吸附作用,受海水氧化性环境影响,可溶性Ce3+和Pt2+分别被氧化成不溶性Ce4+和Pt4+,沉淀被吸附到铁氧化物相中,从而造成富钴结壳稀土和铂族元素的富集。  相似文献   

5.
中太平洋铁锰结壳铅同位素研究   总被引:5,自引:0,他引:5  
已有研究表明大洋中溶解的铅(Pb)来源于陆源物质,但是,对Pb进入大洋的途径争议很大。为此分析了取自中太平洋两块铁锰结壳样品的Pb同位素组成,获得了整个新生代的中太平洋Pb同位素演化历史。结果表明这两块结壳的Pb同位素随时间的演化曲线与中北太平洋沉积物岩心LL44-GPC3中风成碎屑的Pb同位素演化曲线相似。证实该区深水中的天然溶解铅主要来自风成粉尘,并且50Ma之前中太平洋中溶解Pb同位素组成主要取决于源自美洲的风成粉尘的输入,40Ma之后主要取决于源自亚洲的风成粉尘的输入。  相似文献   

6.
太平洋铁锰结壳在中新世以前大多经历了磷酸盐化,一般认为其形成代表了高生产力时期富磷组分对先期已形成结壳的交代作用,即磷酸盐化事件的产物.然而,前人对铁锰结壳磷酸盐化的机制研究多基于点-线分析元素或同位素,对铁锰结壳生长结构及二维元素分布特征研究较少.本研究以西太平洋水成铁锰结壳MDD53为研究对象,利用电子探针(EPM...  相似文献   

7.
中太平洋富钴结壳Co元素地球化学特征   总被引:1,自引:0,他引:1  
对在中太平洋研究区5座海山调查时获取的38个富钴结壳样品中主要金属元素的含量进行了化学分析,探讨了不同海山富钴结壳中Co元素含量的变化规律及结壳中元素间的相关关系,结果表明:(1)5座海山富钴结壳中的各主要金属元素含量相近,38个富钴结壳样品中Co元素的平均含量为0.67%,具有一定的开发前景。(2)不同海山富钴结壳中Co元素含量有一定变化,其变化与富钴结壳的类型、海水水深、地形地貌以及成矿作用等有密切的关系。Co元素在板状结壳中的含量为最高,在钴结核中的含量次之,而在砾状结壳中的含量为最低;富钴结壳中Co元素含量与海水水深呈负相关,浅水区富钴结壳中Co元素的含量明显高于深水区;海山地形地貌对Co元素的含量及富钴结壳的发育有一定影响,海山的椭圆状分支、支脉及边缘部分,Co元素的含量相对较高,富钴结壳发育得较好;Co元素富集成矿作用还主要受锰、铁水成成矿作用的控制。(3)富钴结壳中金属元素之间存在不同程度的相关性。Mn元素分别与Co、Ni、Cu、Zn、Mg、Na、Ba、Ti等元素呈强烈的正相关,而分别与Al、Si、Ca、P、Fe、Sr等元素呈负相关;Co元素分别与Cu、Al、P、Ca等元素呈负相关;Ca元素与P元素呈强烈正相关。  相似文献   

8.
海水的放射成因同位素组成随时间的变化具有提供大陆风化作用、洋底热液活动、大洋环流的变化以及其与构造和气候事件有关系的信息的潜力。所有主要洋盆中铁锰结壳的Sr、Nd和Pb同位素记录已用来研究海水的长期变化。由于分析困难 ,直到现在Hf同位素也没有引起人们的关注。在此 ,我们提供了挖掘自中太平洋海山的两个铁锰结壳的第一个高分辨率和精确的Hf同位素剖面 ,试图限定Hf同位素在中太平洋深水中的演化。目前海水中的Hf同位素组成还不得不直接测定 ,但是可以预料 ,由于以下原因Hf比Nd同位素组成更加易变。第一 ,由地幔…  相似文献   

9.
富钴结壳地球化学与古海洋学研究进展   总被引:7,自引:0,他引:7  
蔡毅华  黄奕普 《台湾海峡》2002,21(2):258-264
本文综述了近年来国内外富钴结壳地球化学与古海洋学研究的新进展,概述了富钴结壳地球化学的研究成果,阐述了富钴结壳中元素的扩散及与周围海水的交换,基岩和磷酸盐化事件对富钴结壳组成的影响,分别介绍了稳定同位素(Pb,Nd和Hf的稳定同位素),放射性同位素(Be,U和Th的放射性同位素)及元素(常量和微量元素,稀土元素)在富钴结壳古海洋学研究上的应用。  相似文献   

10.
对于开阔大洋海山结壳的矿物组成和地球化学特征研究已经比较深入,但对边缘海海山铁锰结壳的研究却较少。以在南海东部管事海山上采集的两块铁锰结壳为研究材料,对其进行了X射线衍射、扫描电镜及电子探针微区的分析,结果显示结壳矿物以水羟锰矿为主,含有少量针铁矿,碎屑矿物主要是石英和长石。结壳的显微结构呈现条带状分布,有10~15μm长的空隙和0.5μm直径大小的孔洞。相对于大洋结壳,结壳的Mn含量较高,与马尼拉海沟附近火山喷发物质有关,但Cu、Co和Ni含量更低,可能与边缘海沉积速率高或有机络合物吸附有关。矿物组成及元素比值表明结壳主要是水成的,但未发生明显磷酸盐化作用。元素比值和相关性表明,Mn主要来源于南海扩张停止后火山喷发、玄武岩风化形成溶解Mn;Fe与Si元素均来自火山碎屑、生源物质和陆源物质,还受到管状蠕虫吸附的影响。南海管事海山结壳是在富氧环境中上升流作用下选择性吸附水体中溶解化学元素缓慢沉积而成。结壳中元素含量随时间变化趋势反映了南海的古环境变化。  相似文献   

11.
铁锰结壳记录了丰富的古海洋和古气候信息,要分析这些信息,必须先确定各壳层的生长年龄。目前主要使用的定年方法有:Be同位素定年、U系同位素定年、Os同位素定年、经验公式法、古地磁地层学方法和古生物地层学方法等。每种定年方法均各有利弊,其中10Be是年龄小于10 Ma结壳的最佳定年方法; U系同位素定年精度高,但定年范围小于0.5 Ma; Os同位素定年时间尺度长,且可以判断沉积间断,但需要有区域的海水Os同位素演化曲线; Co经验公式因为简单易行,是结壳估算年龄最为常用的方法,但该法无法判断沉积间断,在使用时需特别谨慎,应确保经验公式适用于所研究的样品;如果结壳厚度大、生长速率较快且不存在沉积间断,古地磁地层学方法可以快速地进行定年;此外,如果结壳中古生物化石较多,可考虑采用古生物地层学方法。在分析铁锰结壳年代学方法利弊基础上,本文利用U系定年法、古地磁地层学法和经验公式计算法分别对南海铁锰结壳进行定年,通过比较,认为目前铁锰结壳较优的定年方法为古地磁地层学方法。  相似文献   

12.
Based on data on the concentration of noble metals (Au, Ag, Pt, Os, Ir, and Ru) in bulk samples of ferromanganese crusts, the presence of inclusions of micro- and nanosized grains of Ag, Au, Pd, and Pt, often with impurities of other elements, as well as their chaotic distribution, three sources of incorporation of these metals into ore crusts of Far Eastern seas are suggested: seawater, postvolcanic gas–hydrothermal fluids, and hydrothermal plumes. The presence of grains of platinoids and gold in ferromanganese crusts on only some mounts may result from peculiarities in the formation of volcanic rocks on the ancient continental basement.  相似文献   

13.
The 200-mi exclusive economic zone (EEZ) around Johnston Island, 700 mi west of Hawaii, contains economically attractive concentrations of cobalt, nickel, platinum, and rare earth elements contained in manganese crusts on the surface of seafloor plateau areas. Detailed mineralogy and geochemistry reveal these deposits to be largely hydrogenous in origin although also containing elemental additions due to biological, weathering, hydrothermal, detrital, and diagenetic processes. The major mineralogical phase is vernadite (delta manganese dioxide) laid down in strataform crustal deposits. The most valuable metal, cobalt, shows concentrations highest in the upper layers of the crusts and decreasing with stratigraphic depth. Upcoming submersible dives will fully document the significance of this deposit.  相似文献   

14.
Marine hydrogenetically precipitated ferromanganese crusts are widespread in the Pacific Ocean. They occur as pavements coating volcanic or sedimentary hard-rock substrates, mainly on the slopes of seamounts, plateaus and hills in ocean basins and continental margins. We studied three ferromanganese crusts from one dredge haul from the Rivera Plate (western margin of Mexico), which are up to 15 mm thick and grow directly on a substrate of pillow basalt fragments. They consist of laminated, botryoidal, porous aggregates mostly of Fe and Mn oxyhydroxides and up to 10% silicates. XRD analysis showed the predominance of poorly crystallized mineral phases in the crusts that include Mn-feroxyhyte and vernadite, and an authigenic smectite-like clay. Detrital minerals probably derive from granodiorites of the eastern wall of the neighboring Middle America Trench. Scattered barite grains occur on the crust surface and suggest plume fall-out derived from hydrothermal vents, although a possible pelagic source cannot be dismissed. Ratios between major (Fe, Mn, Si) and trace (Co, Ni, Cu) elements reveal that such crusts are predominantly hydrogenetic in origin, although they show a hydrothermal influence that increases in the outer layers. Iron contents range from 16.2 to 25.2 wt.%, and manganese from 3.4 to 14.5 wt.%. The Fe/Mn ratio ranges from 1.6 to 7.0. The SiO2/Al2O3 ratio ranges from 4.3 to 6.6, indicating the presence of biogenic silica (radiolarians). The concentrations of copper (up to 383 ppm) and cobalt (up to 534 ppm) are significantly below those of the typical hydrogenetic crusts, whereas Ni (up to 1320 ppm) is about the same or slightly lower. REE normalized profiles and ΣREE values (486 to 732 ppm) match those reported for hydrogenetic crusts, but suggest a hydrothermal contribution for the later crust layers. The inferred crust growth rates using the Co-chronometer (44 and 229 mm/Myr) are higher than those reported for pure hydrogenetic crusts (mostly 1 to 6 mm/Myr), thus indicating an increasing hydrothermal influence. The highest growth rate (229 mm/Myr, corresponding to the outer crust layers) suggests a regional hydrothermal input of iron and manganese to seawater. The intensification of regional submarine hydrothermal activity began about 13,000 yr ago, and may be related to the tectonic activity in the complex junction of the Rivera, Cocos, Pacific and North America plates.  相似文献   

15.
利用微区XRF技术的大洋固体矿产成分快速无损检测   总被引:1,自引:0,他引:1  
深海固体矿产主要由铁锰结核、富钴结壳和多金属热液硫化物组成,元素在矿产中原位的分布和含量,对了解矿物成因、品位以及评估其经济价值有重要指示作用。本研究利用微区XRF分析技术对铁锰结核、富钴结壳、热液硫化物3种大洋类型矿产样品,进行高分辨、原位和无损的多元素空间分布检测,结果显示了不同元素在3种类型矿物中的空间分布特征。通过对测试数据进一步处理和优化成图流程,可以获得特定元素在矿物中半定量分布图,并对不同元素在矿物空间分布的差异性和相关性进行对比分析,从而建立一种肉眼可见的测试大洋矿产资源样品中元素原位分布的新方法。  相似文献   

16.
The concentration of selenium in marine ferromanganese concretions varies between 0.02 and 1.2 mg kg−1, with an average of 0.6 mg kg−1. This is about two orders of magnitude lower than previously reported. In contrast to minor cationic elements, the concentrations of selenium are relatively uniform between ferromanganese concretions of different origins, except for hydrothermal crusts. It shows the same trends of element enrichment as other oxyanionic elements. The incorporation of selenium into ferromanganese concretions is attributed to adsorption of selenate on iron and manganese oxides.  相似文献   

17.
The elemental composition of ferromanganese sedimentary structures from the bottom of Lake Baikal represented by nodules and crusts, as well as the enclosing sediments, have been studied by the atomic absorption, chemical, and ICP-MS methods. It is established that the contents of the rock-forming and accompanying elements in them are highly variable. In this connection, the examined samples are divided in two groups differing by their Mn/Fe values. In most of the samples, they range from 0.01 to 0.1, although some of the ferromanganese structures or their parts are substantially enriched in manganese. The contents of most of the rare and dispersed elements in the ferromanganese structures are usually at the background level, although the samples maximally enriched in iron or manganese are characterized by relatively high copper, nickel, cobalt, vanadium, zinc, and molybdenum concentrations.  相似文献   

18.
2017年8月中国科学院海洋研究所在西太平洋低纬度海区的卡罗琳洋脊CM4海山开展了多学科综合调查,发现该海山山体表面分布着大量的铁锰结壳。本文对该海山的5个铁锰结壳样品进行了矿物学和地球化学研究,利用X射线衍射(XRD)、电感耦合等离子光谱及质谱(ICP-OES、ICP-MS)等测试技术分析了铁锰结壳的矿物组成、主微量元素和稀土元素含量,并进一步探讨了铁锰结壳的成因类型。结果表明,该海山铁锰结壳的矿物组成以水羟锰矿为主,含有少量钡镁锰矿、水钠锰矿、针铁矿、纤铁矿、石英和方解石。该海山铁锰结壳的Mn、Fe、Co、Ni、Cu元素平均含量分别为24.24%、15.14%、0.16%、0.34%、0.01%。与全球各大洋海山区铁锰结壳相比,该海山样品的Cu含量很低。该海山铁锰结壳的稀土元素(REY)含量相对偏低,总体为轻稀土(LREE)富集;稀土(REY)配分模式显示相对平坦的特征,呈明显的Ce正异常,轻微的Y负异常和Ho正异常。样品的矿物组成、元素比值、元素组合等都表明该海山铁锰结壳属于水成成因,未受明显的成岩作用影响。  相似文献   

19.
In the present paper, iodine(I), iron(Fe), manganese(Mn), cobalt(Co), phosphorus(P) and calcium(Ca)contents in three ferromanganese crusts from the Pacific Ocean are measured by spectrophotometric method and inductively coupled plasma atomic emission spectrometers(ICP-AES) to investigate the contents and distribution of iodine in ferromanganese crusts. The results show that iodine contents in three crusts vary between 27.1 and 836 mg/kg, with an average of 172 mg/kg, and the profile of iodine in the three crusts all exhibits a two-stage distribution zone: a young non-phosphatized zone and an old phosphatized zone that is rich in I, P and Ca. The iodine content ratios of old to young zone in MP5D44, CXD62–1 and CXD08–1 are 2.3, 3.4 and 13.7, respectively.The boundary depths of two-stage zone in MP5D44, CXD62–1 and CXD08–1 locate at 4.0 cm, 2.5 cm and 3.75 cm,respectively, and the time of iodine mutation in three crusts ranges from 17–37 Ma derived from 129 I dating and Co empirical formula, which is consistent with the times of Cenozoic phosphatization events. The present study shows that the intensity of phosphatization is the main responsible for the distribution pattern of iodine in the crusts on the basis of the correlation analysis. Consequently, iodine is a sensitive indicator for phosphatization.  相似文献   

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