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1.
利用主量元素和稀土元素相结合的地球化学方法,对本溪贾家堡子铁矿成矿物质来源和矿床成因进行了研究.结果表明:贾家堡子地区条带状铁矿(BIF)的化学成分主要为TFe2O3和SiO2,并且Al2O3和TiO2含量较低,这一特征与鞍本地区及山西五台山和冀东迁安地区条带状铁矿基本一致,指示该条带状铁矿是由极少碎屑物质加入的化学沉积岩.稀土元素呈现弱轻稀土亏损、重稀土富集的特征,具有明显的Eu正异常特征,表明该BIF的稀土元素来源于火山热液和海水的混合液.贾家堡子地区条带状铁矿床成因类型为Algoma型铁矿.  相似文献   

2.
张朋 《地质与资源》2016,25(1):56-59
通过主量元素和稀土元素相结合的方法,对大台沟铁矿成矿物质来源提出了有效制约.研究表明:大台沟铁矿化学成分主要由TFe2O3和SiO2组成,并且具有较低的Al2O3和TiO2含量,这一特征与鞍本地区及山西五台山和冀东迁安地区铁矿一致,表明大台沟铁矿为火山沉积变质铁矿.稀土元素呈现轻稀土亏损、重稀土富集的特征,具有明显的Eu正异常特征,这些特征表明成矿物质来源于火山热液和海水的混合液.  相似文献   

3.
冀东杏山沉积变质型铁矿床富铁矿成因探讨   总被引:2,自引:0,他引:2  
张龙飞 《地质与勘探》2015,51(3):405-413
本文在野外勘查和岩(矿)相学基础上,对杏山铁矿块状富矿和条带状普通矿石进行主量元素、微量元素和稀土元素等系统研究。杏山铁矿石主要由磁铁矿和石英组成,其中块状富铁矿石相较于条带状普通矿石含有较多的镁铁质矿物,另外块状富矿(XS-60)手标本可见绿泥石化,但镜下蚀变程度较弱,其富矿成因与后期热液蚀变相关度不高;条带状贫矿(XS-10)遭受较强的后期热液蚀变,有一定程度的铁质富集,但仅限于富铁条带,富硅条带未蚀变。矿石中低Al2O3+Na2O含量和Zr、Sc、Th、Hf等含量特征表明杏山铁矿在沉积过程中很少有陆源碎屑加入。微量元素和稀土元素配分模式表明条带状普通矿石和块状富铁矿有共同的成矿物质来源,富铁矿和贫矿都是在缺氧环境下,通过海底热液与海水混合后同沉积形成的,而后期褶皱变形作用使贫矿层加厚的同时,也使富铁层加厚。  相似文献   

4.
辽宁弓长岭铁矿床磁铁矿稀土元素特征及其地质意义   总被引:4,自引:0,他引:4  
辽宁弓长岭铁矿床是我国著名的沉积变质型铁矿床,其二矿区的磁铁富矿达大型规模,属国内之最.为探讨弓长岭铁矿床铁矿的物质来源、形成环境和富矿成因,本文以二矿区六个铁矿体的贫铁矿石和富铁矿石中磁铁矿单矿物为研究对象,利用电感耦合等离子体质谱进行了系统的稀土元素测试.结果表明,所有样品中磁铁矿的稀土元素总量(∑REEs)和Y具有非常一致的特征:稀土元素总量较低,Y/Ho比值较高;经太古界后平均澳大利亚页岩( PAAS)标准化呈现重稀土相对富集、轻稀土相对亏损的分馏模式,大部分呈现La正异常,所有样品都有明显的Eu和Y正异常,这些特征表明研究区的磁铁矿成矿物质主要来源于海底高温热液和海水;虽然磁铁矿的Ce/Ce*为0.69~ 0.97,但大多数样品缺乏真正意义的Ce负异常,这暗示其沉积于还原的海水环境;富铁矿石磁铁矿的稀土元素总量和Eu含量明显高于贫铁矿石的磁铁矿,而且含富矿的上含铁带Eu异常明显较高,表明富铁矿石磁铁矿具有更明显的热液特征,是在贫铁矿石的基础上受热液活动形成的.  相似文献   

5.
莲花山铁矿位于昌邑-安丘铁成矿带的中部,铁矿体赋存于古元古代粉子山群小宋组中。本文通过矿石地球化学特征及其与矽卡岩矿物组合和赋矿围岩结构特征的对比研究,证明了莲花山铁矿与条带状铁矿相似。莲花山铁矿矿石稀土元素含量较低,经页岩标准化的稀土元素配分模式呈现轻稀土元素亏损、重稀土元素富集的特征,具有明显的Eu、Y、La异常,为无明显Ce异常,Y/Ho比值反映了在其沉积时受到海水作用的影响,表明莲花山铁矿的稀土元素来源于火山热液和海水的混合溶液。微量元素中Ti、V、Co、Ni、Mn、Sr、Ba等含量较低,原始地幔标准化的微量元素配分曲线显示,U、La、Hf呈正异常,Ba、Nb、Ta、Sr呈负异常,SiO2/Al2O3、Ti/V、Ni/Co、和Sr/Ba的比值指示了莲花山铁矿成矿物质来源于火山物质的沉积。研究结果表明,莲花山铁矿成矿作用源于火山热液与海水的混合,成矿物质来自火山沉积物,其地质与地球化学特征与五台山铁矿一致,为火山沉积变质型铁矿床。  相似文献   

6.
郭城镇条带状铁矿(BIF)位于胶莱盆地东北缘,赋存于古元古代荆山群变质岩中。通过与冀东迁安和山西五台地区的铁矿对比,可以看出郭城铁矿地球化学特征主要为化学沉积,但有一定量的碎屑参与。在后澳大利亚太古宙页岩(PAAS)稀土配分图中,轻稀土元素亏损、高的Y/Ho值以及La和Y正异常的特征表明铁矿沉淀于海相环境,而高的Sr/Ba、Ti/V值以及Eu的强烈正异常表明火山热液的参与,成矿物质来源于火山活动。无明显的Ce负异常,表明当时可能存在一个缺氧的大气环境。根据矿石及围岩的氢氧同位素值特征,可以看出其成矿作用流体的类型为混合岩化型热液。  相似文献   

7.
辽东大台沟铁矿大地构造单元属中朝准地台胶辽台隆太子河-浑江台陷、辽阳-本溪凹陷,是近年来发现最大的“鞍山式铁矿”。利用LA-ICPMS将含铁层围岩中碎屑锆石年龄限制在2.52~2.56Ga,可推测大台沟铁矿床沉积时代约为2.54Ga左右。全岩分析结果显示SiO2、Fe2O3、FeO的含量占矿石组成的绝大部分,其它组分含量很低,说明矿石极少或者几乎没有受到陆源碎屑物质的混染。Na2O/K2O<1、ω(Sr)/ω(Ba)远远大于1,说明其为海水沉积物。Eu、Y、La具有强烈的正异常,说明形成时有热液参与。赤铁矿石中镜铁矿的发现也说明矿石为后期热液成因的产物。微量元素含量均较低,ΣREE含量较低,LREE亏损,HREE富集,稀土元素La、Eu、Y显示正异常、很高的Y/Ho比,这些特征与其它地区沉积变质型铁矿床非常相似。综合分析认为大台沟沉积变质型铁矿床成矿物质来源海底火山喷发和洋壳,火山活动活跃的部位不利于物质大量沉积,Si、Fe物质依次沉积的同时也陆续的被搬运至适合沉积成矿的位置,形成矿层,经后期区域变质变形作用、变质分异作用形成大台沟沉积变质型铁矿床。  相似文献   

8.
BIF微量稀土元素分析方法及其在冀东司家营铁矿中的应用   总被引:3,自引:2,他引:1  
李文君  靳新娣  崔敏利  王长乐 《岩石学报》2012,28(11):3670-3678
以硅铁条带交替出现为特征的条带状铁建造(BIF)是世界上最重要的铁矿资源类型,精确分析磁铁矿的化学组成具有重要意义。本文开展了磁铁矿样品不同溶样方法分析结果的比对,并详细分析和讨论了冀东司家营铁矿磁铁矿与燧石单条带的微量及REE元素分析的地球化学特征。分析结果表明,对于磁铁矿样品,常规HF+HNO3溶样法与HBr+HNO3组合溶样法具有一致的溶样效果;司家营BIF的Zr,Sc,Th含量极低,表明未受陆源碎屑的污染;铁质与硅质具有低LREE、高HREE、La和Y正异常的海水REE特征,同时具有Eu正异常的热液REE特征;Ce负异常的缺乏,说明当时的古海洋是一个缺氧的环境。研究发现富铁条带的稀土总量大于富硅条带的稀土总量,这可能与硅、铁沉积物的地球化学习性相关,铁质沉积物更易吸收稀土元素。富矿和普通矿石具有原生的热液与海水的混合来源,部分富矿受到后期流体的强烈扰动,甚至表现出热液流体的特征。  相似文献   

9.
铁山河铁矿床赋存于古元古界银鱼沟群地层中,是华北陆块南缘一个重要的富铁矿床。文章对铁山河铁矿床进行了系统的野外地质调查和矿床地球化学研究,并与国内外典型的沉积变质型铁矿床进行了对比。结果显示:铁山河铁矿床保存有明显的化学沉积的特征,化学成分主要由Fe_2O_3、FeO和SiO_2组成,Al_2O_3和TiO_2含量较低;稀土元素总量较低,稀土元素配分模式呈轻稀土元素亏损、重稀土元素富集的特征,具有明显的Eu、Y、La正异常,弱的Ce异常,Y/Ho比值与海水的分布范围相近,Sr/Ba和Ni/Co比值分别与鞍山弓长岭铁矿和山西五台山、冀东迁安地区铁矿相似,但与基性岩浆活动相关的Co、Ni、Cr、V、Ti元素含量相对偏高。这些特征表明:该矿床的形成可能与海相火山沉积物有关,属于火山沉积变质型铁矿的范围,区内基性岩脉广泛发育,矿床可能遭受了后期热液的叠加改造作用;成矿物质来源于热液和海水的混合作用,矿床形成于相对缺氧的环境。  相似文献   

10.
新疆西天山松湖铁矿床磁铁矿成分特征及其成因   总被引:1,自引:0,他引:1       下载免费PDF全文
松湖铁矿位于新疆阿吾拉勒成矿带中段, 其成矿作用经历了2期6个阶段: 硫化物-钾长石阶段、赤铁矿-方解石-绿泥石阶段、磁铁矿-绿泥石-钾长石阶段(称为早阶段铁矿化)、磁铁矿-硫化物阶段(称为晚阶段铁矿化)、方解石-黄铜矿阶段及表生期.为了分析其成分特征及其成因, 使用磁铁矿电子探针分析, 结果显示: 早阶段磁铁矿FeOT含量高, TiO2、Al2O3、MgO、MnO等含量均较低, 与接触交代矿床成分特征相似, 加之SiO2含量较高, 暗示其形成与酸性岩浆热液密切相关; 晚阶段为主成矿阶段, 广泛作用于早阶段矿石之上, 磁铁矿FeOT含量相对较低, TiO2、MnO、V2O3、MgO、Al2O3等含量高于早阶段磁铁矿, 显示为热液成因.综合矿床地质特征, 认为晚阶段磁铁矿形成于岩浆活动晚期或间歇期, 含矿热液中有海水的加入.   相似文献   

11.
通过对出露于西藏南部岗巴—定日地区花岗岩体的地球化学研究表明,岩石中SiO2,Al2O3,Na2O和FeO,MgO等的含量均高,贫CaO和Fe2O3;w(SiO2)介于71.40%~73.06%,A/CNK在1.17~1.34之间,为铝和硅过饱和类型的强过铝质花岗岩。岩石的稀土元素总量(ΣREE)为56.80×10-6~89.12×10-6,(La/Yb)N=6.30~18.26,(La/Sm)N=2.62~3.40,ΣLREE/ΣHREE=2.41~4.66;稀土元素配分曲线呈右倾型,具有弱的负铕异常。Nb,Ti等高场强元素具有明显的亏损,而Rb,U,La,Nd,Hf,Eu,Y等大离子亲石元素具有明显的正异常。岩石的87Sr/86Sr初始比值较高,87Sr/86Sr为(0.738 71~0.751 12)。综合研究认为,本区花岗岩的成因为陆壳部分熔融作用形成的,属陆壳改造型强过铝质花岗岩。本区花岗岩岩浆源区岩石成分主要为砂屑岩,其次为泥质岩,是上地壳部分熔融作用的结果。岩石的微量元素标准化曲线图、岩石地R1-R2图解、Rb-(Yb+Ta)和Rb-(Nb+Yb)图解均显示本区岩体形成于同碰撞构造环境的花岗岩,具有同碰撞岩浆活动的特征,是喜马拉雅早期印度板块与冈底斯板块的俯冲碰撞导致的地壳增厚,上地壳部分熔融的产物;为形成于同碰撞构造环境的花岗岩。  相似文献   

12.
李莹  何保  滕寿仁  邓颖 《矿物岩石》2019,39(1):74-81
为探讨辽宁大台沟铁矿床的成矿物质来源及形成环境,选取典型铁矿石5块进行主量元素、微量元素和稀土元素分析测试。结果显示:大台沟铁矿床保存有明显的化学沉积特征,化学成分主要由Fe_2O_3,FeO和SiO_2组成(Fe_2O_3+FeO+SiO_2=87.33%~96%),其他组分(MnO,MgO,CaO,Na_2O,K_2O,TiO_2,P_2O_5,Al_2O_3)含量较低;页岩标准化后的稀土元素配分曲线显示为稀土总量低(ΣREE平均为19.65×10-6),轻稀土元素相对亏损,重稀土元素相对富集;且具有一定的Eu(Eu/Eu~*=1.52~2.72),Y(Y/Y~*=1.18~1.52),La(La/La~*=1.17~2.26)的正异常,弱的Ce(Ce/Ce~*=0.79~0.92)异常;Y/Ho值平均34.19接近于海水的分布范围;Sr/Ba值平均1.79,属于火山岩和海相沉积物;Ti/V值平均38.84,属于火山建造。这些特征表明:该矿床的形成可能与海相火山沉积物有关,属于火山沉积变质型铁矿范围;成矿物质来源于热水和海水的混合作用;矿床形成于相对于缺氧的环境。  相似文献   

13.
上庄坪铅锌银矿床是新一轮国土资源大调查中在北秦岭二郎坪群发现的硫化物矿床。笔者通过对矿床矿石、容矿同岩、重晶石岩的微量、稀土元素地球化学特征分析和地质特征研究,探讨成矿构造环境、成矿物质来源及矿床成因问题。研究表明.矿石和容矿围岩稀土元素球粒陨石标准化组成模式均为右倾型.矿石与围岩在Cu-Pb-Zn判别图解中投点区域一致.矿石Zn/(Zn Pb)与冲绳海槽和上向黑矿矿石特征相似、与TAG和EPR13°N区硫化物存在差异.矿石具较高As、Sb和Pb与低Cu、Cd和Se元素特征.认为该矿床成矿元素来源于壳幔混合、但以壳源为主的围岩变(石英)角斑岩和变细碧岩。矿石稀土元素、微量元素地球化学特征、矿床地质特征及与热水沉积重晶石岩和硅质岩的紧密共生关系说明,上庄坪矿床是弧后盆地构造环境海底热液喷流成岩成矿作用的产物。重晶石岩、硅质岩、矿床纵向和横向分带是寻找和勘探该类矿床的重要标志和依据。  相似文献   

14.
The iron isotope, trace and major element compositions of Eoarchean supracrustal rocks from southern West Greenland (Isua Supracrustal Belt, the islands of Akilia and Innersuartuut) were analyzed in order to identify protoliths and characterize the imprints of metamorphism and metasomatism. Banded iron formations (BIFs) from the Isua Supracrustal Belt (ISB) have trace element characteristics that are consistent with seawater derivation, including high Y/Ho ratios, positive Eu/Eu anomalies, positive La/La anomalies, and concave upward REE patterns. These rocks also have heavy Fe isotopic compositions relative to surrounding igneous rocks (∼+0.4‰/amu). The most likely interpretation is that this signature was inherited from partial oxidation in a marine setting of Fe emanating from a source similar to modern mid-ocean ridge hydrothermal vents (∼−0.15‰/amu).Banded quartz-rich rocks from the island of Akilia with high Fe/Ti ratios share many similarities with bona fide BIFs from Isua (heavy Fe isotopic compositions up to +0.4‰/amu, elevated Y/Ho ratios compared to igneous rocks, sometimes positive Eu/Eu anomalies) suggesting a chemical sedimentary origin.Iron-poor metacarbonates from the southwestern part of the ISB have light Fe isotopic compositions (∼−0.4‰/amu). This is consistent with derivation of these rocks by fluid flow through surrounding ultramafic rocks and deposition as metasomatic carbonates. Iron-rich metacarbonates from the northwest and northeast parts of the ISB have Fe isotopic compositions (from +0.1 to +0.4‰/amu) and trace element patterns (high Y/Ho ratios, positive Eu/Eu and La/La anomalies, and concave upward REE) similar to associated BIFs. The most likely interpretation is that these iron-rich metacarbonates were derived from mobilization of Fe in BIFs by metasomatic fluids.  相似文献   

15.
Modern chemical sediments display a distinctive rare earth element + yttrium (REE + Y) pattern involving depleted LREE, positive La/La*SN, Eu/Eu*SN, and YSN anomalies (SN = shale normalised) that is related to precipitation from circumneutral to high pH waters with solution complexation of the REEs dominated by carbonate ions. This is often interpreted as reflecting precipitation from surface waters (usually marine). The oldest broadly accepted chemical sediments are c. 3,700 Ma amphibolite facies banded iron-formation (BIF) units in the Isua supracrustal belt, Greenland. Isua BIFs, including the BIF international reference material IF-G are generally considered to be seawater precipitates, and display these REE + Y patterns (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004). Greenland Eoarchaean BIF metamorphosed up to granulite facies from several localities in the vicinity of Akilia (island), display REE + Y patterns identical to Isua BIF, consistent with an origin by chemical sedimentation from seawater and a paucity of clastic input. Furthermore, the much-debated magnetite-bearing siliceous unit of “earliest life” rocks (sample G91/26) from Akilia has the same REE + Y pattern. This suggests that sample G91/26 is also a chemical sediment, contrary to previous assertions (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004), and including suggestions that the Akilia unit containing G91/26 consists entirely of silica-penetrated, metasomatised, mafic rock (Fedo and Whitehouse 2002a). Integration of our trace element data with those of Bolhar et al. (Earth Planet Sci Lett 222:43–60, 2004) demonstrates that Eoarchaean siliceous rocks in Greenland, with ages from 3.6 to 3.85 Ga, have diverse trace element signatures. There are now geographically-dispersed, widespread examples with Isua BIF-like REE + Y signatures, that are interpreted as chemically unaltered, albeit metamorphosed, chemical sediments. Other samples retain remnants of LREE depletion but are beginning to lose the distinct La, Eu and Y positive anomalies and are interpreted as metasomatised chemical sediments. Finally there are some siliceous samples with completely different trace element patterns that are interpreted as rocks of non-sedimentary origin, and include metasomatised mafic rocks. The positive La/La*SN, Eu/Eu*SN and YSN anomalies found in Isua BIFs and other Eoarchaean Greenland samples, such as G91/26 from Akilia, suggests that the processes of carbonate ion complexation controlling the REE − Y patterns were already established in the hydrosphere at the start of the sedimentary record 3,600–3,850 Ma ago. This is in accord with the presence of Eoarchaean siderite-bearing marbles of sedimentary origin, and suggests that CO2 may have been a significant greenhouse gas at that time.  相似文献   

16.
Banded Iron Formations(BIFs) are chemical sediments, ubiquitously distributed in the Precambrian supracrustal belts; thus their trace element compositions are helpful for deciphering geochemical evolution on the Earth through time. However, it is necessary to elucidate factors controlling the whole-rock compositions in order to decode the ancient seawater compositions because their compositions are highly variable. We analyzed major and trace element contents of the BIFs in the 3.8-3.7 Ga Isua supracrustal belt(ISB), southern West Greenland. The BIFs are petrographically classified into four types:Black-,Gray-, Green-and White-types, respectively. The Green-type BIFs contain more amphiboles, and are significantly enriched in Co, Ni, Cu, Zn, Y, heavy rare earth element(HREE) and U contents. However,their bulk compositions are not suitable for estimate of seawater composition because the enrichment was caused by secondary mobility of metamorphic Mg, Ca and Si-rich fluid, involvement of carbonate minerals and silicate minerals of olivine and pyroxene and/or later silicification or contamination of volcanic and clastic materials. The White-type BIFs are predominant in quartz, and have lower transition element and REE contents. The Gray-type BIFs contain both quartz and magnetite. The Black-type BIFs are dominated by magnetite, and contain moderate to high transition element and REE contents. But,positive correlations of V, Ni, Zn and U contents with Zr contents suggest that involvement of detrital,volcanic and exhalative materials influences on their contents. The evidence for significant influence of the materials on the transition element contents such as Ni in the BIFs indicates the transition element contents in the Archean ocean were much lower than previously estimated. We reconstructed secular variations of V,Co, Zn and U contents of BIFs through time, which show Ni and Co contents decreased whereas V, Zn and U contents increased through time. Especially, the Ni and Co contents drastically decreased in the Mesoarchean rather than around the Great Oxidation Event. On the other hand, the V,Zn and U contents progressively increased from the Mesoarchean to the Proterozoic. Stratigraphical trends of the BIFs show increase in Y/Ho ratios and decrease in positive Eu anomaly upwards, respectively. The stratigraphic changes indicate that a ratio of hydrothermal fluid to seawater component gradually decrease through the deposition, and support the Eoarchean plate tectonics, analogous to the their stratigraphic variations of seafloor metalliferous sediments at present and in the Mesoarchean.  相似文献   

17.
甘肃夏河地区印支期埃达克岩的厘定及其意义   总被引:6,自引:0,他引:6       下载免费PDF全文
对出露于甘肃夏河地区,隶属西秦岭的印支晚期复式岩体的地质地球化学研究表明。其岩石具有与典型埃达克岩相似的特征:SiO2多数(72%~58%),高Al2O3(16.7%~14.6%),Sr多数大于(400×10^-6),低Y(16×10^-6~7×10^-6)和Yb(1.7×10^-6~0.56×10^-6),明显亏损Nb和Ta,稀土元素分异强烈,富集LREE,低HREE,并有较弱的Eu负异常(δEu为0.9~0.4)在(La/Yb)N-Yb和Sr/Y-Y图解上样品主要落入埃达克质岩区域。该套埃达克质岩的厘定,对研究秦岭造山带晚古生代古特提斯洋的构造演化、地球动力学特征具有重要意义。  相似文献   

18.
贵州松桃西溪堡锰矿沉积地球化学特征   总被引:4,自引:0,他引:4  
贵州黔东断裂坳陷带是贵州重要的锰矿成矿带,并发育新元古代大塘坡期的一套完整“黑色岩系”,锰矿主要赋存于该黑色岩系中。本文以松桃西溪堡锰矿床为例,通过岩石学、矿物学、地球化学等研究方法,探讨这类锰矿床的成矿物质来源及成因。研究表明矿石中的矿物组分复杂,结构构造类型多样,富集As、Sb、Ag、Co、Mo、W、Cs和Ba等元素,Fe/Ti、(Fe+Mn)/Ti、A1/(AI+Fe+Mn)、Y/Ho、Nb/Ta比值,以及Cr.zr和Th.u图解均揭示成矿过程中有热水物质参与;V/(V+Ni)、V/Cr比值表明锰矿形成于缺氧环境;稀土元素分布模式、Ce、Eu异常及La.Ce、La/Yb.EREE图解显示锰矿形成于被动大陆边缘环境,并具有热水沉积特征。因此,古被动大陆边缘是锰矿富集的理想场所,热水(液)活动为其提供了丰富的物质来源。这为锰矿的找矿拓展了新的思路。  相似文献   

19.
根据矿物组成白云鄂博矿区的碳酸岩岩可墙可分为白云石型、白云石-方解石共存型和方解石型三种类型。REE和微量元素地球化学表明,这三类碳酸岩岩墙为碳酸岩浆演化不同阶段的产物,白云石型和白云石-方解石共存型对应于早期岩浆阶段,其(La/Nd)n、(La/Yb)n比值随稀土总量的增加而增大,方解石型则对应于碳酸岩浆演化的晚期热液阶段,其稀土总量明显富集,但其(La/Nd)n、(La/Y)n和(La/Yb)n比值随稀土总量的增加却有减小的趋势,热液阶段也是白云鄂博稀土矿化的主要阶段。  相似文献   

20.
Abstract. Rare earth, major and trace element geochemistry is reported for the Kunimiyama stratiform ferromanganese deposit in the Northern Chichibu Belt, central Shikoku, Japan. The deposit immediately overlies greenstones of mid-ocean ridge basalt (MORB) origin and underlies red chert. The ferromanganese ores exhibit remarkable enrichments in Fe, Mn, P, V, Co, Ni, Zn, Y and rare earth elements (excepting Ce) relative to continental crustal abundance. These enriched elements/ Fe ratios and Post-Archean Average Australian Shale-normalized REE patterns of the ferromanganese ores are generally analogous to those of modern hydrothermal ferromanganese plume fall-out precipitates deposited on MOR flanks. However in more detail, Mn and Ti enrichments in the ferromanganese ores are more striking than the modern counterpart, suggesting a significant contribution of hydrogenetic component in the Kunimiyama ores. Our results are consistent with the interpretation that the Kunimiyama ores were umber deposits that primarily formed by hydrothermal plume fall-out precipitation in the Panthalassa Ocean during the Early Permian and then accreted onto the proto-Japanese island arc during the Middle Jurassic. The presence of strong negative Ce anomaly in the Kunimiyama ores may indicate that the Early Permian Panthalassa seawater had a more striking negative Ce anomaly due to a more oxidizing oceanic condition than today.  相似文献   

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