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1.
用化学方法和ICP-MS方法分别对中、西太平洋海山富钴铁锰结壳产出区玄武岩的主元素、微量元素和稀土元素(REE)含量进行了测定,结果表明,研究区玄武岩经受了强烈的洋底低温蚀变作用,主元素成分发生了明显的变化,失去了原岩的特征.样品与新鲜大洋岛屿玄武岩(OIB)极为相似的稀土元素配分模式和微量元素含量特征表明,所研究的岩石属典型的大洋板内玄武岩.受洋底低温蚀变作用的影响,样品的Al2O3,Fe2O3,MnO、K2O,P2O5含量增加,MgO,FeO的含量降低.蚀变作用使大洋岛屿玄武岩中的镁、铁等活动组分大量流失,从而表现出相对富SiO2的特征(标准矿物计算结果中出现石英).由于蚀变作用,活动组分的流失使样品的REE相对富集,而富REE铁锰氧化物在玄武岩气孔和裂隙中的沉淀不仅使样品的REE含量增大,而且引起轻稀土元素(LREE)与重稀土元素(HREE)分馏,表现为∑c(Ce)/∑c(Yb)值增大.以REE富集机制为基础,对样品中铁锰氧化物的沉淀量和单位质量新鲜玄武岩中活动组分的流失量进行了理论计算,结果表明,因低温蚀变作用所引起的新鲜玄武岩的单位质量亏损为0.150~0.657,而单位质量新鲜玄武岩中铁锰氧化物的沉淀量为0.006~0.042.主元素中以铁、镁的流失亏损最为明显,新鲜玄武岩中铁、镁的流失比例分别为18.28%~70.95%和44.50%~93.94%,超过了岩石总量的流失亏损比例(15.0%~65.7%),因而样品相对贫铁、镁.其他元素的流失量和流失比例都很好地印证了地球化学研究的结果.样品中铝、钾、磷负的流失量是由于沸石在岩石气孔中的充填和岩石的磷酸盐化.理论计算结果和地球化学研究都表明,大洋岛屿玄武岩的低温蚀变向海水提供了大量金属,这是大洋海水中金属循环的重要环节.  相似文献   

2.
Ferromanganese nodules and crusts contain relatively high concentration of rare earth elements(REE) and yttrium(REY),with a growing interest in exploitation as an alternative to land-based REY resources.On the basis of comprehensive geochemical approach,the abundance and distribution of REY in the ferromanganese nodules from the South China Sea are analyzed.The results indicate that the REY contents in ferromanganese deposits show a clear geographic regularity.Total REY contents range from 69.1×10~(–6) to 2 919.4×10~(–6),with an average value of 1 459.5×10~(–6).Especially,the enrichment rate of Ce content is high,accounting for almost 60% of the total REY.This REE enrichment is controlled mainly by the sorption of ferromanganese oxides and clay minerals in the nodules and crusts.Moreover,the total REY are higher in ferromanganese deposits of hydrogenous origin than of diagenetic origin.Finally,Light REE(LREE) and heavy REE(HREE) oxides of the ferromanganese deposits in the study area can be classified into four grades: non-enriched type,weakly enriched type,enriched type,and extremely enriched type.According to the classification criteria of rare earth resources,the Xisha and Zhongsha platform-central deep basin areas show a great potential for these rare earth metals.  相似文献   

3.
The major elements, trace elements, K-Ar age and Sr-Nd-Pb isotopic systems of the Cenozoic volcanic rocks in Daheishan Island and Cishan, Penglai, Shandong Province are measured. The volcanic rocks ( olivine-nephelinite and nepheline-basanite ) in DaheishanIsland erupted periodically in an interval of 0.32 Ma, from 8.72 Mm 8.39 Ma, 8.08 Ma to 7.73Ma. The volcanic rocks are all rich in light REEs. They are similar to the OIB-type alkali basalt in the trace elements normalized model by primordial mantle: rich in high field elements such as Nb and Ta, and imcompatible elements such as Cs, Rb, Ba, Th, U. The volcanic rocks show a depletion of K and Rb elements. It is suggested by the trace elements that the olivine-nephelinite in Daheishan Island is originated fi‘om deep resources under the continental mantle, ε Nd (0) values of the volcanic rocks in Daheishan Island and Cishan are 5.31 - 8.51 and 7.33 respectively, suggesting that the volcanic rocks are from the depleted mantle resources, which have higher Sm/Nd ratios than the CHUR. ^143Nd /^144Nd ratios of Daheishan Island olivine-nephelinite and Cishan alkali basalts are 0.512 910 - 0.513 074 and 0.513 014 resoeetivelv. The ^87Sr /^86Sr of Daheishan lsland volcanic rocks are lower than that of Cishan, 0.703 427 - 0.703 482 and 0.703 895 respectively. The Daheishan Island olivinenephelinite has the Pb isotopic values as follows: ^206Pb /^204pb= 18.028 9 ~17.972 8,^207Pb /^204Pb= 15,435 8 - 15.402 2 and ^208Pb /^204Pb=38.087 6 - 37.997 5, lower than those of Cishan basanite. The Cishan basanite has ^206Pb / ^204Pb = 18.240 1, ^208Pb /^204Pb = 15.564 5 and ^208Pb /^204Pb=38.535. The authors suggest that the olivine-nephelinite in Daheishan Island is similar to the E-type MORB or Hawaii OIB, and the alkali basalts in Cishan similar to the Kerguelen OIB. The dominant mantle components of DM PREMA and perhaps DM( Dupal type ) are the dominant mantle components for volcanic rocks in Daheishan Island and Cishan. The PREMA component plays an important role.  相似文献   

4.
西南印度洋中脊是典型的慢速扩张洋中脊之一。对采自西南印度洋中脊50°E附近的7件玄武岩和蛇纹石化橄榄岩样品所作的分析表明,基性玄武岩类SiO2含量为43.72%~48.40%,TiO2含量较少,为1.14%~1.52%;MgO含量为5.96%~10.98%;TFe2O3含量为4.55%~5.2%;Mg#值为0.53~0.64,里特曼指数σ为2.34~20.10。微量元素Zr/Nb和Y/Nb比值为显示N-MORB的性质,但是其他微量元素的比值(Ba/Nb,Ba/Th,La/Nb,Nb/U,Nb/Pb)均不显示正常洋中脊玄武岩的特征,微量元素原始地幔标准化蛛网图显示强烈富集K和Pb,亏损Nb,稀土元素显示较为平缓的分配模式。超基性蛇纹石化橄榄岩的主量元素特征为SiO2为38.91~45.49;TiO2含量为0.02~0.28;MgO含量很高,为36.87~40.61,TFe2O3含量为2.82~3.91,Mg#值为0.92~0.94。微量元素中Ni,Cr的含量很高,原始地幔标准化蛛网图显示橄榄岩强烈富集K和Pb,Ba,Th,La,Ce,Ti中等程度富集,而亏损Nb,Sr。稀土元素总量较低,标准化曲线显示轻稀土元素富集模式。结合地球化学特征及前人研究资料分析认为,西南印度洋中脊的基性岩和超基性岩属同源性质,其原始地幔物质可能为部分正常洋中脊亏损地幔混染了陆壳或远洋沉积物的结果。  相似文献   

5.
利用X射线荧光法和ICP-MS等方法对取自超慢速扩张的西南印度洋脊(SWIR) 49.6°E热液区的热液产物和玄武岩样品进行元素地球化学特征分析研究,结果表明:(1)与亏损型洋中脊玄武岩(N-MORB)相比,研究区玄武岩样品的主量元素组成显示其偏碱性,而微量元素对比表明该区玄武岩明显富集Pb元素;(2)对热液产物的综合分析表明这些样品多为Fe-Si-Mn氧羟化物且都为热液来源;(3)热液产物的∑REE含量介于玄武岩和海水之间,经球粒陨石标准化的稀土元素(REE)分布模式均表现出Eu正异常和轻稀土(LREE)富集的特征。另外,本研究还表明,利用玄武岩和热液产物地球化学指标不仅能够模拟出以热液喷口为中心的元素地球化学晕,而且能反映出热液活动的影响范围。  相似文献   

6.
南海海盆15°N附近呈东西向展布的珍贝-黄岩海山被认为是32~17Ma前南海海盆的残留扩张中心.对采自黄岩海山的两个火山岩样品(9DG,9DG-2)进行了岩石学、地球化学和年代学研究.两个样品的SiO2含量分别为60.3%和63.6%,Al2O3含量分别为17.56%和17.55%,TiO2含量分别为0.48%和0.31%,碱度率分别为3.88和3.62.根据岩石学和岩石化学分类,样品属碱性系列的粗面岩.对稀土元素和微量元素分析表明岩石具有洋岛玄武岩(OIB)型配分型式,轻重稀土总量比(∑c(LREE)/∑c(HREE))和球粒陨石标准化镧镱比((La/Yb)N)分别高达17.22和27.23,并具有铕负异常和锶、磷、钛亏损的特点.样品9DG的锶-钕-铅同位素分析结果为锶-87的含量与锶-86的含量之比值为0.704183,钕-143的含量与钕-144的含量之比值为0.512827,铅-206的含量与铅-207的含量之比值为18.68668,铅-207的含量与铅-204的含量之值为15.67962,铅-208的含量与铅-204的含量之比值为39.00261,表明初始岩浆来自软流圈地幔,具有与珍贝海山玄武岩相似的同位素组成.经钾-氩法测年,粗面岩的年龄为(7.77±0.49)Ma,略晚于珍贝海山玄武岩的年龄[(9.1±1.29)~10.0±1.80Ma],属于南海扩张期后晚中新世火山活动的产物.对比珍贝海山玄武岩的地球化学和同位素特征,认为两者有相同的岩浆源区,但是它们经历了不同程度的结晶分异过程,在晚中新世期间珍贝-黄岩海山可能有地幔柱活动.  相似文献   

7.
对采自西南印度洋中脊(SWIR)50°E附近5个站位的玄武岩样品进行了岩石学和元素地球化学研究。样品主量元素、TAS分类图解和AFM图解显示,SWIR研究区样品类型主要为低钾拉斑玄武岩。相对原始地幔SWIR区玄武岩具有Ba、Nb、Sr负异常,K表现为正异常。稀土元素分配模式均为左倾型,具有轻微的Eu、Ce正异常;SWIR区玄武岩都起源于上地幔,SWIR玄武岩则明显向EMⅡ端元偏移。SWIR玄武岩地幔源区相对最为富集,可能为DM和EMⅡ的混合源区,存在少量的陆壳成分。研究区玄武质岩浆起源深度为尖晶石橄榄岩区域处于中度还原环境下,经历了明显的橄榄石+单斜辉石+斜长石的分离结晶。  相似文献   

8.
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   

9.
东菲律宾海表层沉积物中元素的赋存状态   总被引:2,自引:0,他引:2  
为了解东菲律宾海不同类型表层沉积物中元素的赋存状态,采用化学提取方法对有无新型铁锰结壳发育站位表层沉积物样品进行了分级提取及测试,不同类型表层沉积物中成矿和稀土元素的赋存状态总体一致,表明研究区表层沉积物形成于相似的地质和海洋环境中。成矿元素中Fe绝大部分赋存在残渣态中,Mn、Cu、Co和Ni则主要赋存在铁锰氧化物结合态中,稀土元素也主要赋存在这两个相态中,碳酸盐结合态、铁锰氧化物结合态和有机结合态对重稀土元素优先吸附或具络合作用,引起重稀土元素的相对富集和铈的负异常,残渣态优先吸附轻稀土元素,导致轻稀土元素的富集和铈的正异常,火山物质则使表层沉积物残渣态表现出铕的正异常特征。同时,不同表层沉积物样品间也存在一定的差异,这与其局部形成条件——铁锰结壳发育与否有关。  相似文献   

10.
The REE compositions of hydrothermal deposits and basalt samples from the Southwest Indian Ridge (SWIR) were determined with ICP-MS.The results show that there are significant differences between different types of samples although all samples show relative LREE enrichment.The contents of REE in hydrothermal sulfides and alterated rocks samples are lower (from 7.036 × 10 6 to 23.660 × 10 6),while those in the white chimney deposits are relatively higher (ranging from 84.496 × 10 6 to 103.511 × 10 6).Both of them are lower than basalts.Chondrite-normalized REE distribution patterns show that sulfides and alterated rocks samples are characterized by significant positive Eu anomalies.On the contrary,white chimney deposits have obvious negative Eu anomalies,which may be caused by abundant calcite existing in the white chimney samples.Both the content and distribution pattern of REE in sulfides suggest that REE most possibly is originally derived from hydrothermal fluids,but influenced by the submarine reducing ore-forming environment,seawater convection,mineral compositions as well as the constraint of mineral crystallizations.  相似文献   

11.
The Okinawa Trough(OT) is a back-arc basin at an initial spreading stage that is under the influence of subduction of the Philippine Sea Plate. In this study, we analyzed the geochemical compositions of basaltic glass in the OT and discussed the effects of different magmatic sources, evolution, and subducted components in basalts. Our results showed that the middle and southern regions of the OT exhibit characteristics consistent with an iron-rich tholeiite series. Trace element proportions conform to the typical spider diagram pattern characteristic of back-arc basin basalts, rich in large ion lithophile elements(LILEs) including Rb, Ba, Pb, U, and Th, while depleted in high field-strength elements(HFSEs) including Nb, Ta, Zr, Hf, and Ti. The distribution of rare earth elements(REEs) is also consistent with enrichment by right-leaning light rare earth elements(LREEs).The addition of enriched mantle type I(EMI) materials as well as mantle heterogeneity may have led to variable degrees of enrichment in different regions. The magma source of the middle trough has undergone crystallization towards pyroxene, while development of plagioclase was restricted partly, and the crystallization of spinel and olivine ceased altogether. At the same time, crystallization of the southern OT magma source was dominated by olivine and including the formation of plagioclase, pyroxene, and magnetite(or titanomagnetite). Finally, the results of this study showed that 90% Th, 95% Ba in the southern basalt, 50%–70% Th and 70%–90% Ba in the middle basalt originated from subducted component. Different subducted component influence may be due to different subduction zone structural feature.  相似文献   

12.
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   

13.
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   

14.
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   

15.
冲绳海槽岩浆源的三分量混合模型   总被引:1,自引:0,他引:1  
综合分析了冲绳海槽玄武岩中微量元素的地球化学特征,发现最少要求三分量混合作用来解释其岩浆源成分,并通过最大方差因子分析估算了3个分量的贡献比例。亏损型地幔是海槽岩浆源的主体,但其中舍有富集型地幔的成分,尤其是海槽中部玄武岩岩浆源中这种富集型地幔成分的特征表现得更为明显。俯冲组分是岩浆源中的另一个主要成分,贡献量为20%左右,是造成海槽区玄武岩中Pb强烈富集的重要原因。  相似文献   

16.
Some of the islets in the eastern Beibu Gulf are covered by Quaternary volcano strata. The rock samples from these islets mainly consist of quartz tholeiites (at Shenjiandao), olivine tholeiites (at Linshidao and Xieyang- dao) and alkali basalts (at Yangpubi and Jianshidao), and basically represent four periods of the Quaternary volcanism of Hainan Island and its adjacent regions. Except for the samples from Shenjiandao, most of the Quaternary volcanics of these islets belong to alkali magma series. The trace element characteristics of all of these samples show they are OIB (oceanic island basalt) -like, which implies that their deep geodynamic setting may be related to a mantle plume. The Sr-Nd-Pb isotopic compositions show that the mantle source beneath the Quaternary strata can be regarded as a result of binary mixing between a depleted, DMM (de- pleted MORB mantle)-like source and an enriched mantle type 2 (EM2). The EM2 may be originated from the Hainan mantle plume, and has been metasomatized by carbonaceous fluids released from ancient re- cycled oceanic crust at an asthenospheric mantle level. These features, together with typical trace element ratios, reflect that the parent magma was not subjected to crustal contamination during its ascent to the surface. This study provides further petrological and geochemical evidence for the existence of the Hainan mantle plume.  相似文献   

17.
The concentrations of rare earth elements (REEs), sulphate, hydrogen sulphide, total alkalinity, calcium, magnesium and phosphate were measured in shallow (<12 cm below seafloor) pore waters from cold-seep sediments on the northern and southern summits of Hydrate Ridge, offshore Oregon. Downward-decreasing sulphate and coevally increasing sulphide concentrations reveal sulphate reduction as dominant early diagenetic process from ~2 cm depth downwards. A strong increase of total dissolved REE (∑REE) concentrations is evident immediately below the sediment–water interface, which can be related to early diagenetic release of REEs into pore water resulting from the re-mineralization of particulate organic matter. The highest pore water ∑REE concentrations were measured close to the sediment–water interface at ~2 cm depth. Distinct shale-normalized REE patterns point to particulate organic matter and iron oxides as main REE sources in the upper ~2-cm depth interval. In general, the pore waters have shale-normalized patterns reflecting heavy REE (HREE) enrichment, which suggests preferential complexation of HREEs with carbonate ions. Below ~2 cm depth, a downward decrease in ∑REE correlates with a decrease in pore water calcium concentrations. At this depth, the anaerobic oxidation of methane (AOM) coupled to sulphate reduction increases carbonate alkalinity through the production of bicarbonate, which results in the precipitation of carbonate minerals. It seems therefore likely that the REEs and calcium are consumed during vast AOM-induced precipitation of carbonate in shallow Hydrate Ridge sediments. The analysis of pore waters from Hydrate Ridge shed new light on early diagenetic processes at cold seeps, corroborating the great potential of REEs to identify geochemical processes and to constrain environmental conditions.  相似文献   

18.
We present new major element, ICP-MS trace element, and Sr–Nd–Pb isotope data of basalts from four locations along the Carlsberg Ridge (CR), northern Indian Ocean. The basalts are low-K tholeiites with 7.52–9.51 wt% MgO, 49.40–50.60 wt% SiO2, 0.09–0.27 wt% K2O, 2.55–2.90 wt% Na2O, and 0.60–0.68 Mg#. Trace element contents of the basalts show characteristics similar to those of average normal MORB, such as LREE depleted patterns with (La/Sm)N ratio of 0.55–0.69; however, some samples are enriched in large-ion lithophile elements such as K and Rb, suggesting probable modification of the mantle source. Poor correlations between the compatible elements [e.g. Ni, Cr, and Sr (related to olivine, clinopyroxene and plagioclase, respectively)] and the incompatible elements (e.g. Zr and Y), and positive correlations in the Zr versus Zr/Y and Nb versus Nb/Y plots suggest a magmatic evolution controlled mainly by mantle melting rather than fractional crystallization. Our results extend the CR basalt range to higher radiogenic Pb isotopes and lower 143Nd/144Nd. These basalts and basalts from the northern Indian Ocean Ridge show lower 143Nd/144Nd and higher 87Sr/86Sr values than those of the depleted mantle (DM), defining a trend towards pelagic sediment composition. The Pb isotopic ratios of basalts from CR 3–4°N lie along the compositional mixing lines between the DM and the upper continental crust. However, the low radiogenic Pb of basalts from CR 9–10°N lie on the mixing line between the DM and lower continental crust. Since the Pb isotopic ratio of MORB would decrease if the source mantle was contaminated by continental lithospheric mantle, we suggest that CR contains continental lithospheric material, resulting in heterogeneous mantle beneath different ridge segments. The continental lithospheric material was introduced into the asthenosphere before or during the breakup of the Gondwana. These results support the long-term preservation of continental material in the oceanic mantle which would significantly influence the isotopic anomaly of the Indian Ocean MORB.  相似文献   

19.
The circulation of methane-rich fluids at cold seeps often leads to the precipitation of seep carbonates close to the seafloor along continental margins, which can be used as records of past fluid seepage. Rare earth element (REE) concentrations in seep carbonates have been used to trace fluid sources and provide information on associated biogeochemical processes at cold seeps. The REE concentrations of a series of carbonates collected from cold seeps in the southwestern Dongsha area of the northern South China Sea are analyzed in this study. The total REE contents (ΣREE) of the seep carbonates analyzed show a wide variation from 17 ppm to 523 ppm with an average ΣREE value of 54 ppm, which are higher than the typical marine carbonate values of ∼28 ppm commonly reported and also higher than those of the carbonates from other cold seep areas. A positive correlation between Fe–Mn content and ΣREE was observed. These results suggest that the seep carbonates of this study were primarily controlled by the methane-derived fluid from which they precipitated. The Fe-rich dolomite and siderite, which are the main components of the carbonates, are responsible for the enrichment of the REE. A slight positive Ce anomaly observed in the shale-normalized REE patterns of the studied seep carbonates suggests that they formed in anoxic conditions, and the correlations between Ce/Ce* and LaN/SmN, Ce/Ce* and DyN/SmN, Ce/Ce* and ΣREE further reveal that the REE characteristics of most seep carbonate samples preserve the original redox conditions in which they precipitated and late diagenesis has had little effect on the REE. However, the REE characteristics of sub-samples DS2-2B, DS1-6A and DS1-7A are very different from those of the other sub-samples, indicating a greater impact of late diagenesis and post-oxidation favored REE enrichment.  相似文献   

20.
V Marchig  H Gundlach 《Marine Geology》1981,40(3-4):M35-M43
111 samples of diagenetically aged radiolarians sampled in the Central Pacific manganese nodules belt were investigated chemically and microscopically.

Authigenic clays of the smectite group are precipitated in the cavities of radiolarian tests; metal oxides are precipitated on the surfaces of radiolarian tests. During these processes a separation of iron from manganese takes place: about 96% of the iron is bound to smectites and all of the manganese is bound to the oxide coatings of the radiolarians.

With further diagenesis, radiolarian tests are dissolved together with their oxide coatings. This dissolution of the oxide coatings provides material for the growth of manganese nodules, material which is depleted in Fe and enriched in Mn, Cu, and Zn.

The smectite aggregates that fill the cavities of radiolarian tests contain iron bound to their crystal lattice. Whereas radiolarian tests are dissolved during the diagenesis, these smectite aggregates do not dissolve and thus become enriched in older samples.  相似文献   


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