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1.
Geochemical Fingerprint and Iron Ore Potential of the Siliceous Itabirite from Palaeoproterozoic Nyong Series,Zambi Area,Southwestern Cameroon 
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下载免费PDF全文 Sylvestre Ganno Cyriel Moudioh Adjija Nzina Nchare Gus Djibril Kouankap Nono Jean Paul Nzenti 《Resource Geology》2016,66(1):71-80
The study area forms part of an emerging iron ore province of southern Cameroon. Geochemistry analyses reveal that the siliceous itabirite has a very simple chemical composition, with Fe2O3 and SiO2 representing more than 96 wt.% of the average composition; suggesting chemical precipitates of silica and iron. Low Al2O3 and TiO2 concentrations and a weak positive correlation between them point to a minor detrital component in the precipitated marine sediments. The Si/Al ratio (average 52.7) indicates the hydrothermal origin of the studied itabirite. The Al–Si discrimination diagram supports this interpretation through the plot of all data in the hydrothermal field. The studied samples have low iron content (about 39.32% Fe), high gangue content (40.97% SiO2 and 1.3 % Al2O3) and low concentration of the deleterious elements (0.16 % P and < 0.01% S). The main gangue mineral is silica which can be efficiently removed from iron ores during preparation of raw materials for the blast furnace process. According to commercial standards for crude iron ores, it may be concluded that the Zambi iron ores are a low‐grade magnetic ore that can be profitably exploited for the production of iron for steel production. 相似文献
2.
Genesis of superimposed hypogene and supergene Fe orebodies in BIF at the Madoonga deposit, Yilgarn Craton, Western Australia 总被引：1，自引：0，他引：1
The Madoonga iron ore body hosted by banded iron formation (BIF) in the Weld Range greenstone belt of Western Australia is a blend of four genetically and compositionally distinct types of high-grade (>55 wt% Fe) iron ore that includes: (1) hypogene magnetite–talc veins, (2) hypogene specular hematite–quartz veins, (3) supergene goethite–hematite, and (4) supergene-modified, goethite–hematite-rich detrital ores. The spatial coincidence of these different ore types is a major factor controlling the overall size of the Madoonga ore body, but results in a compositionally heterogeneous ore deposit. Hypogene magnetite–talc veins that are up to 3 m thick and 50 m long formed within mylonite and shear zones located along the limbs of isoclinal, recumbent F1 folds. Relative to least-altered BIF, the magnetite–talc veins are enriched in Fe2O3(total), P2O5, MgO, Sc, Ga, Al2O3, Cl, and Zr; and depleted in SiO2 and MnO2. Mafic igneous countryrocks located within 10 m of the northern contact of the mineralised BIF display the replacement of primary igneous amphibole and plagioclase, and metamorphic chlorite by hypogene ferroan chlorite, talc, and magnetite. Later-forming, hypogene specular hematite–quartz veins and their associated alteration halos partly replace magnetite–talc veins in BIF and formed during, to shortly after, the F2-folding and tilting of the Weld Range tectono-stratigraphy. Supergene goethite–hematite ore zones that are up to 150 m wide, 400 m long, and extend to depths of 300 m replace least-altered BIF and existing hypogene alteration zones. The supergene ore zones formed as a result of the circulation of surface oxidised fluids through late NNW- to NNE-trending, subvertical brittle faults. Flat-lying, supergene goethite–hematite-altered, detrital sediments are concentrated in a paleo-topographic depression along the southern side of the main ENE-trending ridge at Madoonga. Iron ore deposits of the Weld Range greenstone belt record remarkably similar deformation histories, overprinting hypogene alteration events, and high-grade Fe ore types to other Fe ore deposits in the wider Yilgarn Craton (e.g. Koolyanobbing and Windarling deposits) despite these Fe camps being presently located more than 400 km apart and in different tectono-stratigraphic domains. Rather than the existence of a synchronous, Yilgarn-wide, Fe mineralisation event affecting BIF throughout the Yilgarn, it is more likely that these geographically isolated Fe ore districts experienced similar tectonic histories, whereby hypogene fluids were sourced from commonly available fluid reservoirs (e.g. metamorphic, magmatic, or both) and channelled along evolving structures during progressive deformation, resulting in several generations of Fe ore. 相似文献
3.
The Coniacian-Santonian high-phosphorus oolitic iron ore at Aswan area is one of the major iron ore deposits in Egypt. However, there are no reports on its geochemistry, which includes trace and rare earth elements evaluation. Texture, mineralogy and origin of phosphorus that represents the main impurity in these ore deposits have not been discussed in previous studies. In this investigation, iron ores from three localities were subjected to petrographic, mineralogical and geochemical analyses. The Aswan oolitic iron ores consist of uniform size ooids with snowball-like texture and tangentially arranged laminae of hematite and chamosite. The ores also possess detrital quartz, apatite and fine-grained ferruginous chamosite groundmass. In addition to Fe2O3, the studied iron ores show relatively high contents of SiO2 and Al2O3 due to the abundance of quartz and chamosite. P2O5 ranges from 0.3 to 3.4 wt.% showing strong positive correlation with CaO and suggesting the occurrence of P mainly as apatite. X-ray diffraction analysis confirmed the occurrence of this apatite as hydroxyapatite. Under the optical microscope and scanning electron microscope, hydroxyapatite occurred as massive and structureless grains of undefined outlines and variable size (5–150 μm) inside the ooids and/or in the ferruginous groundmass. Among trace elements, V, Ba, Sr, Co, Zr, Y, Ni, Zn, and Cu occurred in relatively high concentrations (62–240 ppm) in comparison to other trace elements. Most of these trace elements exhibit positive correlations with SiO2, Al2O3, and TiO2 suggesting their occurrence in the detrital fraction which includes the clay minerals. ΣREE ranges between 129.5 and 617 ppm with strong positive correlations with P2O5 indicating the occurrence of REE in the apatite. Chondrite-normalized REE patterns showed LREE enrichment over HREE ((La/Yb)N = 2.3–5.4) and negative Eu anomalies (Eu/Eu* = 0.75–0.89). The oolitic texture of the studied ores forms as direct precipitation of iron-rich minerals from sea water in open space near the sediment-water interface by accretion of FeO, SiO2, and Al2O3 around suspended solid particles such as quartz and parts of broken ooliths. The fairly uniform size of the ooids reflects sorting due to the current action. The geochemistry of major and trace elements in the ores reflects their hydrogenous origin. The oolitic iron ores of the Timsha Formation represent a transgressive phase of the Tethys into southern Egypt during the Coniacian-Santonian between the non-marine Turonian Abu Agag and Santonian-Campanian Um Barmil formations. The abundance of detrital quartz, positive correlations between trace elements and TiO2 and Al2O3, and the abundance mudstone intervals within the iron ores supports the detrital source of Fe. This prediction is due to the weathering of adjacent land masses from Cambrian to late Cretaceous. The texture of the apatite and the REE patterns, which occurs entirely in the apatite, exhibits a pattern similar to those in the granite, thus suggesting a detrital origin of the hydroxyapatite that was probably derived from the Precambrian igneous rocks. Determining the mode of occurrence and grain size of hydroxyapatite assists in the maximum utilization of both physical and biological separation of apatite from the Aswan iron ores, and hence encourages the use of these ores as raw materials in the iron making industry. 相似文献
4.
辽冀地区(主要包括鞍山-本溪地区和冀东地区)位于华北克拉通东北部,产出有诸多BIFs型大型-特大型铁矿床。鞍山-本溪地区和冀东地区是我国最大的两个铁矿集区,其中鞍本地区铁矿储量占全国的24%左右,冀东地区铁矿资源储量占全国的10%以上。虽然辽冀地区BIFs大多为形成于新太古代绿岩带中的Algoma型BIFs,但不同矿区BIFs形成环境和受后期改造的程度不一致,鞍本地区BIFs变质级别为绿片岩相-角闪岩相,冀东地区BIFs经历了绿片岩相-麻粒岩相的变质作用,且辽冀地区普遍发育混合岩化。本文主要对比研究了辽冀地区28个铁矿床200件铁矿石的主量元素特征,为探讨辽冀地区BIFs的形成提供了更多的信息。BIFs样品主要由SiO2和Fe2O3T组成,其中鞍山-本溪地区SiO2+Fe2O3T平均为95.10%,冀东地区SiO2+Fe2O3T平均为88.06%,CaO和MgO含量仅次于SiO2和Fe2O3T,且大部分矿区具有正相关关系,Al2O3、TiO2、K2O、Na2O、MnO、P2O5含量很低,这暗示BIFs原岩为一种化学沉积岩,主要为含有少量碳酸盐泥的硅质和铁质的胶体沉积;辽冀地区Al2O3和TiO2均可见明显的正相关,这可能是由于BIFs沉积过程中有少量碎屑物质的加入,这种相关性在冀东地区更为明显,且除SiO2+Fe2O3T外,其它氧化物含量明显高于鞍本地区,说明冀东地区BIFs形成时沉积环境更为动荡,有更多的碎屑物质加入;虽然辽冀不同地区BIFs经历了不同级别的变质作用,形成了不同的矿物组合,但是氧化物含量却变化不大,这说明了变质反应主要为等化学反应;鞍本地区和冀东地区碱质含量也存在差异性,前者的Na2O和K2O含量均低于后者,且后者Na2OK2O,结合野外地质特征,可能暗示了混合岩化作用对冀东地区的影响更为显著。 相似文献
5.
The oolitic ironstones ore deposit of Jebel Ank (central Tunisia), is a simply folded stratiform ore body of about 2.5–8 m thickness located in the upper part of the epicontinental Souar Formation (Late Eocene) and is covered by the continental Segui Formation (Mio-Pliocene). The deposit contains about 20 Mt of ore with an average grade of 50% Fe. Generally, oolitic iron deposition occurs in shallow water lagoonal environments. The Jebel Ank deposit lies between two regional disconformities (Late Eocene and Miocene), and is evidence of a transitional stage at the end of regional regression before renewed transgression. The footwall of the oolitic iron ore-bearing bed consists of a fine-grained sandstone bed (10–20 cm-thick) pinching out laterally westward into green clays. The hanging wall is composed of thin-bedded limestone and clay alternations (2–3.5 m-thick).Iron occurs in the form of cryptocrystalline goethite with limited Al-Fe substitution. The goethite contains around 48% Fe, 5% Al and up to 1.5% P. Jarosite, alunite and manganese minerals (cryptomelane, psilomelane and manjiorite) are supergene secondary minerals, probably related to descending surface fluids. These manganese minerals occur as accessory minerals with the goethite and are most abundant at the lowermost part of the succession showing varied morphologies (local cement, space filling and free centimeter sized nodules). Fe-oolites in the deposit are similar to those documented in many other oolitic ironstone deposits. The dominant Fe-oolite type (>90%) has a concentrically laminated cortex with no nucleus. The nuclei of the oolites that do have a nucleus are most commonly detrital quartz grains.Major elements in high grade samples (Fe2O3 > 65%) vary within a limited range and show higher concentrations of SiO2 (average 7.85%) and Al2O3 (average 5.1%), with minor TiO2, MnO, MgO, Na2O, K2O, and SO3 (less than 1%). PAAS-normalized trace elements of bulk samples and Fe-oolite generally show similar behavior, both are enriched in V, Co, Ni, Mo, As, Zn, and Y and are depleted in Cu, Rb, Zr, Nb, Ba, and Hf. Anomalous V, Cr, Ni, Zn, and REE-Y are correlated with goethite. PAAS-normalized REE-Y patterns of both bulk samples and Fe-oolite show slight HREE enrichment, positive Ce with negative Y anomalies.The mineralogy (goethite and cryptomelane) along with the geochemistry (Si vs. Al; As + Cu + Mo + Pb + V + Zn vs. Ni + Co binary plots; Zn–Ni–Co triangular diagram, REE-Y content and patterns and Ce/Ce1 vs. Nd and Ce/Ce1 vs. YN/HoN binary plots) of the studied oolitic ironstone are congruent with a hydrogenetic type. While two possible sources of iron for Jebel Ank ironstone can be proposed: (i) submarine weathering of glauconite-rich sandstone and (ii) detrital iron from adjacent continental hinterland, the later is the more plausible source of iron, based on paleogeographic setting, the occurrence of fine sandstone underlying the iron level, occurrence of Mn-ores in the lower part of the Fe-ores succession, high phosphorous, zinc, ∑REE-Y concentrations and Y/Ho ratios, and low La/Ce ratios. 相似文献
6.
广西平果上二叠统合山组沉积型铝土矿储量大,并以伴生稀散元素Ga为特色。从主量成分和微量元素角度研究平果铝土矿的地球化学特征、形成环境及其与Ga的相互关联性,对综合回收利用和提升矿床经济价值有重要帮助。通过对整个研究区内均匀采集的18件不同类型的矿石及铝土岩样品进行金属Ga和常量、微量元素测试,经统计学方法计算和相关性图解分析,发现样品中Ga平均含量已达到工业品位（0.002×10-2）。但在不同类型矿石中的富集程度不同:豆鲕粒状铝土矿>致密块状铝土矿>铝土岩。而且Ga含量与Al2O3含量呈显著正低相关性;与SiO2含量呈显著负相关关系;与V含量呈显著正低相关关系;与稀土元素相关性不强,无明显规律性。通过对那豆沉积型铝土矿床古地理环境和不同类型样品Sr/Ba比值、Ga的富集、LREE/HREE比值分析发现:区内沉积型铝土矿主成矿期为较稳定、酸性、潮湿的滨海至浅海相环境;而且从二叠纪合山组早期的滨海相氧化环境逐步过渡到二叠纪合山组后期的浅海相还原环境。矿石类型则由早期的紫红色致密块状矿化变化为青灰色至灰黑色鲕粒状矿化。 相似文献
7.
新疆赞坎铁矿床位于西昆仑塔什库尔干地块西段,是近年新发现的一个大型沉积变质型磁铁矿床。赋矿岩系布伦阔勒群主要由黑云母石英片岩、斜长角闪片岩、变粒岩、硅质岩及磁铁石英岩等组成。目前探明工业矿体4条,单个矿体长度大于2.5km,矿体厚10~70m;局部见高品位铁矿段(mFe50%),长度达900m,厚度40m左右。矿石类型主要为2种,一种为原生的条纹-条带状磁铁矿(为主);另一种为热液改造形成的块状(高品位铁矿石)及浸染状磁铁矿。矿石稀土元素配分(PAAS)表明,原生条纹-条带状铁矿石Ce和Y元素异常不明显(~1.15、~0.94),Eu具正异常(~1.69),Y/Ho平均值为25,稀土配分模式与沉积变质型铁矿相似。而受改造的矿石中,浸染状矿石具有较高的稀土总量,明显富集轻稀土,La和Ce显示正异常(~1.46、~1.17),Y显示负异常(=0.66~0.72),Eu表现为强烈的正异常(~4.37),稀土配分模式明显不同于原生条纹-条带状铁矿石。矿体围岩斜长角闪片岩(变沉积岩)中的碎屑锆石U-Pb年龄为591±1Ma,结合前人对矿区内侵入体的年代学研究(霏细斑岩,533Ma),大致反映沉积铁矿的形成时代为新元古代至早寒武世。电子探针显示,条带状磁铁矿中的TiO_2、AL_2O_3、MgO、MnO含量较低,标型组分含量与沉积变质型磁铁矿颇为接近,在磁铁矿单矿物成因图解中,条带状磁铁矿整体显示磁铁矿为沉积变质型铁矿;浸染状矿石和块状矿石的组成与典型沉积变质型铁矿的偏离反映了后期岩浆-构造热事件对条带状铁矿石的改造;上述结果显示赞坎铁矿整体属于沉积变质型铁矿(BIF)。调查发现赞坎高品位铁矿体与早寒武世侵入的霏细斑岩联系密切,高品位矿石及其围岩发育一定程度的矽卡岩化,如阳起石化、碳酸盐化和黄铁矿化。本文推测高品位铁矿石的成因可能为霏细斑岩的岩浆热液溶解并运移早期沉积变质铁矿中的含铁物质,在构造发育处充填交代形成块状磁铁富矿石。在早寒武世侵入到矿区中部的霏细斑岩体中,同时发育有角砾状磁铁矿和脉状磁铁矿,因此,岩浆热液改造原生条带状铁矿石形成高品位铁矿石的时代应为早寒武世。 相似文献
8.
9.
Kersten Löwen Guido Meinhold Arzu Arslan Talip Güngör Jasper Berndt 《International Geology Review》2020,62(4):389-414
ABSTRACTSiliciclastic sediments from the Upper Palaeozoic Konya Complex and its Mesozoic cover were studied by a multi-method approach combining thin-section petrography, bulk-rock geochemistry, mineral chemistry of rutile, and U–Pb geochronology of detrital zircons. Provenance sensitive data of samples from the Upper Palaeozoic Hal?c? Formation indicate sediment supply from mainly low- to medium-grade metamorphosed sedimentary rocks of felsic character, while the contribution from volcanic rocks was rare. The detrital zircon record of sediments from the Hal?c? Formation documents sediment supply from different sources and excludes a similar provenance. Some samples show great similarities with Palaeozoic sandstones from the cover sequence of the Saharan Metacraton and the Arabian–Nubian Shield, while the other samples indicate a provenance that must be sought in units with a southern Eurasian affinity. The upper limit for sediment deposition in the Hal?c? Formation is mostly constrained by Early Palaeozoic zircon populations; however, sediment accumulation in Pennsylvanian–Cisuralian time is more likely, contemporaneously with the Upper Palaeozoic succession on the Karaburun Peninsula (western Turkey). The provenance of sediments from the Upper Triassic Ard?çl? Formation remains enigmatic, but the source should be sought nonetheless in units close to the depositional site. In any case, detrital zircon age spectra and compositional data exclude recycling of underlying rock units (i.e. Hal?c? Formation). Overall, our new provenance data reveal great similarities between the Konya Complex and comparable units (Chios, Karaburun) but also highlight distinct differences in terms of sediment composition and provenance. 相似文献
10.
Duncan Large 《Journal of Geochemical Exploration》1981,15(1-3)
A total of 138 samples of the Devonian sediments in the vicinity of the Tom stratiform Pb-Zn-Ba deposit were analysed for major elements and 16 minor and trace elements by X-ray fluorescence.The geochemistry of the footwall argillites is characterised by a concentration of elements that are typically associated with the detrital resistate minerals and feldspars (e.g. Al2O3, Na2O, K2O, TiO2, Ce, Nb, Zr), which are contained within the interbedded silty layers of probable distal turbidite origin.The hanging-wall shales are characterised by high V concentrations. The C-organic data and the V/Cr ratios suggest that sapropelic conditions may have been locally developed in the vicinity of the West zone mineralisation and in the hanging-wall shales. Very high concentrations of Ba were found to be present in the hanging-wall shales (>0.5% Ba).Zn is more widely dispersed than Pb in the sediments around the mineralisation. There is no marked enrichment of Fe, Mn or Cu in the sediments close to the mineralisation. 相似文献
11.
P. Halbach 《Mineralium Deposita》1972,7(2):141-153
Zusammenfassung Die sedimentären Eisenerze bei Trstenik (Kosovo-Metohija) enthalten im Mittel ca. 40% Fe, 1,0% Ni und 3,5% Cr2O3. Stratigraphisch liegt das linsenförmige Erzlager zwischen liegenden paläozoischen Serpentin-Peridotiten und hangenden oberkretazischen Sedimenten. Die Erze sind als Umlagerungs-produkte einer lateritischen Verwitterungskruste von Serpentiniten im Rahmen der Oberkreidetransgression entstanden. Ein Vergleich der chemischen Zusammensetzung von bergfrischem und oberflächennahem Erz belegt den exogenen Einfluß der Verwitterung durch typische Elementver-schiebungen. Die in lateritischen Verwitterungsprofilen von Serpentiniten meist vorliegende räumliche Trennung der Metalle Fe, Ni, Co und Cr ist durch den marinen Umlagerungsvorgang weitgehend aufgehoben worden. Der Mineralbestand des normalen Erztyps sowie seine Herkunft werden beschrieben und diskutiert. Quantitativ wichtige Mineralphasen sind Brauneisenerz, Spinelle, Karbonate, Quarz sowie Serpentin und seine Zersetzungs-produkte. Ni ist teilweise, Co fast ausschließlich an Millerit gebunden. Die Anwesenheit von Sulfiden neben Eisenspat und Chamosit weist auf reduzierende Bedingungen im frühdiagenetischen Zustand. Weitere Ni-Träger können Hydrosilikate oder auch Brauneisenerz bzw. Tonminerale der Grundmasse sein. Im Gegensatz zu genetisch ähnlichen Ni-haltigen Trümmereisenerzen in Griechenland (Larymna) hat eine spätere Migration von Nickel in liegende Basisbereiche des Erzlagers hier nicht stattgefunden.
Sedimentary iron ore near Trstenik (Kosovo-Metohija) contains an average of about 40% Fe, 1.0% Ni and 3.5% Cr2O3. The lenticular deposit is situated between underlying Paleozoic serpentine-peridotites and overlying Upper Cretaceous sediments. The ore is a redepositional product of a lateritic weathering crust of serpentinite formed during the Upper Cretaceous transgression. A comparison of the chemical composition of fresh ore with ore close to the surface proves the exogenous influence of recent weathering by typical shifting of elements. In laterite profiles of serpentinites, the metals Fe, Ni, Co and Cr are mostly seperated and enriched in different layers; by the marine redeposition this characteristic feature was largely eliminated. The mineral content of the normal ore type and its origin is described and discussed. Minerals of quantitative importance are limonite, spinels, carbonates, quartz and serpentine with its weathering products. Ni is partially, Co is almost completely bound to millerite. The presence of several sulfides beside iron carbonate and chamosite indicates a reducing environment in an early diagenetic stage. Further Ni-bearing phases can be hydrosilicates or limonit or, respectively, clay minerals of the matrix. Contrary to Ni-bearing, detrital iron ore of similar origin in Greece (Larymna) a later migration of Ni to deeper parts of the deposit was not observed in this case.相似文献
12.
Age and grade of metamorphism of the considerable iron deposit of Hajigak (Central Afghanistan) have been controversial until now. A recent field study on the eastern part of the district produced new data concerning the geological environment and paragenesis of the ore. The iron beds are situated in the Upper Kalu Formation (= Awband Suite) of lower Paleozoïc, may be Silurian to Lower Devonian age. Basic lavas and tuffs, converted into green-schists, always are present near the ore bodies; and straight relationship is evident between basic rocks and iron ore. We consider the succession of events at Hajigak to be as follows: — at the bottom of a Paleozoïc sedimentary basin, an andesitic submarine volcanism brought along tuffs, lavas, and sericitic and chloritic sediments of exhalative origin; in the same time, hematite and magnetite precipitated. — afterwards gabbro and dolerite sills were intruded; as a result, iron oxides were remobilized, filling fractures across gabbro boundaries, and replacing neighbouring dolomites. — at last, but before Upper Devonian, Lower Paleozoïc rocks of Hajigak and Turkman area were affected by two kinds of metamorphism: the first one, of green-schist facies, is contemporaneous with magmatic activity; the second one, sericitic dynamo-metamorphism, appeared when the folding took place, mainly in the eastern region (Khesh and Zerok areas). In conclusion, the Hajigak iron ore appears to be a submarine — exhalative deposit, synchronous with a Lower Paleozoïc basic volcanic activity (but non ophiolitic). 相似文献
13.
岩石学、沉积相、元素地球化学的综合分析结果表明,羌塘盆地沃若山地区上三叠统土门格拉组(T_3t)地层为三角洲沉积;整体富含水解性元素、Fe族元素以及上部砂岩Fe元素富集(高Fe/Mn比值)的特征表明古水体环境为较浅的河口-滨岸环境;CIA值(63.8~79)、ICV值(0.52~1.4)和Ga/Rb-K2O/Al2O3关系图解分析结果显示当时为风化强度中等、较温暖的半干旱—半湿润气候;Sr/Ba比值全部小于1(0.09~0.27),表明沉积水体为盐度较低的陆相淡水;根据V、U、Mo的含量比值,判断其为氧化-弱氧化的富氧水体环境。较为温湿的气候有利于生物的繁殖,但氧化-弱氧化的环境不利于有机质的富集,限制了该地区烃源岩发育:土门格拉组烃源岩的TOC含量为0.76%~1.46%(均值为1.04%),属中等品质的烃源岩。 相似文献
14.
鞍本地区大孤山条带状铁建造含铁矿物和相分带特征及形成环境分析 总被引：1，自引：1，他引：0
鞍山-本溪条带状铁建造(Banded Iron Formation,简称BIF)位于华北克拉通东北缘,是世界上典型BIF之一,也是我国最重要的铁矿资源基地。大孤山位于鞍山地区南部矿带,为新太古代典型的Algoma型BIF,与华北克拉通其它大多数BIF相比,具有较低变质程度(绿片岩相-低角闪岩相)和较完整的沉积相分布特征。因此,通过大孤山BIF的研究有利于追踪Algoma型BIF的原生矿物组成及其后期成岩-变质过程,进而通过分析原生矿物形成的物理化学条件探讨古海洋环境。依据原生矿物共生组合及产出特征,可将大孤山BIF沉积相划分为氧化物相(30%)、硅酸盐相(50%)和碳酸盐相(20%)。氧化物相主要分布于主矿体南部,主要矿物组成为磁铁矿和石英;硅酸盐相分布于主矿体中部,主要矿物组成除了石英和磁铁矿之外,还有黑硬绿泥石、绿泥石、镁铁闪石等;碳酸盐相分布于矿体北部,主要矿物组成为菱铁矿、磁铁矿和石英等。本文通过大孤山BIF岩相学观察和含铁矿物化学成分研究,推测原生沉积物的组成为无定形硅胶、三价铁氢氧化物和富铝粘土碎屑,在经历了成岩和低级变质作用后转变为具不同相带的条带状铁建造。通过分析磁铁矿、菱铁矿和黑硬绿泥石等矿物在不同P_(O_2)-P_(CO_2)和pH-Eh条件下的共生相图可知,这些矿物均是在较低氧逸度、中到弱碱性环境下形成。综合考虑矿物成分、共生组合及受变质作用较弱等信息,本文推测制约原生矿物形成的控制因素主要是古海水氧化还原状态、酸碱度、CO_2含量和硫逸度。 相似文献
15.
宁乡式沉积铁矿床的时空分布和演化 总被引：20，自引：0，他引：20
宁张式铁矿是我国最重要的沉积型铁矿床,广泛分布于我国南部的鄂、湘、赣、川、滇、黔、桂诸省以及甘南地区。含矿建造主要赋存于中上泥盆统,而以上泥盆统为主,可划分出７个成矿区,其中最重要的鄂西－湘西北成矿区。在１个矿床中通常有１～４层铁矿,其中有１个是主矿层,矿石主要由鲕状赤铁矿组成,次有菱铁矿、鲕绿泥石和褐铁矿,含铁品位一般为３０％～４５％,含磷通过偏高,介于０．４％～１．１％,中泥盆世和晚泥盆世沉积铁矿在分布范围、矿床规模、赋太和围岩建造和矿石特征等方面有一定差异,文章对鄂西－湘西北成矿区的矿宋时空演化作了重点论述,对铁矿的分布与岩相古地理的关系及矿床生成条件进行了讨论,指出含矿建造大多产于海侵程序的沉积岩系中,在湿热环境下较封闭或半封闭的古海盆,古海湾或潮坪中的浅海－滨海相沉积组合是有利的成矿古地理条件,提出要 相似文献
16.
云南拖顶一带的泥盆纪地层,由于受构造的影响呈断块产出。通过对矿区泥盆纪地层的详细研究,认为其地层层序较为清楚,可以分出下泥盆统碎碎岩、中泥盆统碳酸盐岩和上泥盆统碎屑岩－碳酸盐岩。在斩野外实地考察和室内研究的基础上,本文详细厘定子泥盆纪的沉积相,并恢复了岩相古地理格局。进而建立了该区的层序地层格架,分为５个沉积层序,并对沉积体系与拖顶铜矿的关系进行了探讨。 相似文献
17.
The Neoproterozoic (593–532 Ma) Dahongliutan banded iron formation (BIF), located in the Tianshuihai terrane (Western Kunlun orogenic belt), is hosted in the Tianshuihai Group, a dominantly submarine siliciclastic and carbonate sedimentary succession that generally has been metamorphosed to greenschist facies. Iron oxide (hematite), carbonate (siderite, ankerite, dolomite and calcite) and silicate (muscovite) facies are all present within the iron-rich layers. There are three distinctive sedimentary facies BIFs, the oxide, silicate–carbonate–oxide and carbonate (being subdivided into ankerite and siderite facies BIFs) in the Dahongliutan BIF. They demonstrate lateral and vertical zonation from south to north and from bottom to top: the carbonate facies BIF through a majority of the oxide facies BIF into the silicate–carbonate–oxide facies BIF and a small proportion of the oxide facies BIF.The positive correlations between Al2O3 and TiO2, Sc, V, Cr, Rb, Cs, Th and ∑REE (total rare earth element) for various facies of BIFs indicate these chemical sediments incorporate terrigenous detrital components. Low contents of Al2O3 (<3 wt%), TiO2 (<0.15 wt%), ∑REE (5.06–39.6 ppm) and incompatible HFSEs (high field strength elements, e.g., Zr, Hf, Th and Sc) (<10 ppm), and high Fe/Ti ratios (254–4115) for a majority of the oxide and carbonate facies BIFs suggest a small clastic input (<20% clastic materials) admixtured with their original chemical precipitates. The higher abundances of Al2O3 (>3 wt%), TiO2, Zr, Th, Cs, Sc, Cr and ∑REE (31.2–62.9 ppm), and low Fe/Ti ratios (95.2–236) of the silicate–carbonate–oxide facies BIF are consistent with incorporation of higher amounts of clastic components (20%–40% clastic materials). The HREE (heavy rare earth element) enrichment pattern in PAAS-normalized REE diagrams exhibited by a majority of the oxide and carbonate facies BIFs shows a modern seawater REE signature overprinted by high-T (temperature) hydrothermal fluids marked by strong positive Eu anomalies (Eu/Eu1PAAS = 2.37–5.23). The low Eu/Sm ratios, small positive Eu anomaly (Eu/Eu1PAAS = 1.10–1.58) and slightly MREE (middle rare earth element) enrichment relative to HREE in the silicate–carbonate–oxide facies BIF and some oxide and carbonate facies BIFs indicate higher contributions from low-T hydrothermal sources. The absence of negative Ce anomalies and the high Fe3+/(Fe3+/Fe2+) ratios (0.98–1.00) for the oxide and silicate–carbonate–oxide BIFs do not support ocean anoxia. The δ13CV-PDB (−4.0‰ to −6.6‰) and δ18OV-PDB (−14.0‰ to −11.5‰) values for siderite and ankerite in the carbonate facies BIF are, on average, ∼6‰ and ∼5‰ lower than those (δ13CV-PDB = −0.8‰ to + 3.1‰ and δ18OV-PDB = −8.2‰ to −6.3‰) of Ca–Mg carbonates from the silicate–carbonate–oxide facies BIF. This feature, coupled with the negative correlations between FeO, Eu/Eu1PAAS and δ13CV-PDB, imply that a water column stratified with regard to the isotopic omposition of total dissolved CO2, with the deeper water, from which the carbonate facies BIF formed, depleted in δ13C that may have been derive from hydrothermal activity.Integration of petrographic, geochemical, and isotopic data indicates that the silicate–carbonate–oxide facies BIF and part of the oxide facies BIF precipitated in a near-shore, oxic and shallow water environment, whereas a majority of the oxide and carbonate facies BIFs deposited in anoxic but Fe2+-rich deeper waters, closer to submarine hydrothermal vents. High-T hydrothermal solutions, with infusions of some low-T hydrothermal fluids, brought Fe and Si onto a shallow marine, variably mixed with detrital components from seawaters and fresh waters carrying continental landmass and finally led to the alternating deposition of the Dahongliutan BIF during regression–transgression cycles.The Dahongliutan BIF is more akin to Superior-type rather than Algoma-type and Rapitan-type BIF, and constitutes an additional line of evidence for the widespread return of BIFs in the Cryogenian and Ediacaran reflecting the recurrence of anoxic ferruginous deep sea and anoxia/reoxygenation cycles in the Neoproterozoic. In combination with previous studies on other Fe deposits in the Tianshuihai terrane, we propose that a Fe2+-rich anoxic basin or deep sea probably existed from the Neoproterozoic to the Early Cambrian in this area. 相似文献
18.
19.
The Middle–Upper Jurassic boundary in the westernmost Tethyan basins is marked by a discontinuity. A thin iron crust with ferruginous ooids and pisoids and an overlying ferruginous oolitic limestone lithofacies occur in a genetic relationship to this discontinuity with a reduced thickness (< 50 cm) and very local distribution in the Prebetic Zone (Betic Cordillera).The ferruginous coated grains are subdivided into two types. Type A ooids are characterised by thin, regular lamination in concentric layers enclosing a nucleus; they are dominant in the top of the iron crust (100% of the ferruginous ooids) and in the ferruginous oolitic limestone (82%). Type B ooids typically have thick, irregular lamination in a few discontinuous concentric layers enclosing a variable nucleus including bioclasts and foraminifera; they are exclusive to the ferruginous oolitic limestone (18% of the ferruginous ooids). The bulk chemical composition varies between 80% Fe2O3 by weight in the iron crust and 67% by weight in the coated grains. In the ferruginous ooids, the contents in SiO2 (5.4%), Al2O3 (6.5%), P2O5 (3.6%), and CaO (4.7%) are higher than in the crust. Trace elements (V, Cr, Co, Ni, Zn, Y, Mo, and Pb) in both the crust and ooids show enriched values compared with the bulk composition of the upper continental crust. The mineral composition of the iron crust and ooids is primarily goethite, with small amounts of Al-hydroxide (bohemite) and apatite, whereas hematite is identified only in the iron crust.The Type A ooids are interpreted as having an origin related to the iron crust. Since there is no evidence to support a marine genesis for the iron crust, the possibility of a subaerial origin is presented here. The crust has characteristics (chemical and mineralogical composition) similar to those of ferruginous pisolitic plinthite (highly weathered redoximorphic soil), and goethite shows an Al-substitution range (5–10 mol%) that indicates pedogenic conditions. Soil processes under periodic hydrous conditions are suggested; groundwater soils with hydrous conditions are congruent with the formation of the Type A ferruginous ooids and pisoids. In this situation, a coastal plain with periodically flooded soils would be the likeliest scenario. Callovian shallow carbonate shelf was possibly emerged and weathered, followed by marine sedimentation during the Middle Oxfordian, associated with major flooding of the Prebetic shelf and the erosion of ferruginous pisolitic plinthite. The first marine deposit was ferruginous oolitic limestones. Fragments of iron crust and Type A ferruginous ooids were reworked and incorporated into the marine sediments. A second phase of ferruginous ooids (Type B) with clear marine features developed, benefiting from iron-rich microenvironments due to the redistribution from iron crust fragments and Type A ferruginous ooids. 相似文献
20.
A. I. Brusnitsyn V. N. Kuleshov E. N. Perova A. N. Zaitsev 《Lithology and Mineral Resources》2017,52(3):192-213
The paper presents the results of study of ferromanganese carbonate rocks in the Sob area (Polar Urals), which is located between the Rai-Iz massif and the Seida–Labytnangi Railway branch. These rocks represent low-metamorphosed sedimentary rocks confined to the Devonian carbonaceous siliceous and clayey–siliceous shales. In terms of ratio of the major minerals, ferromanganese rocks can be divided into three varieties composed of the following minerals: (1) siderite, rhodochrosite, chamosite, quartz, ± kutnahorite, ± calcite, ± magnetite, ± pyrite, ± clinochlore, ± stilpnomelane; (2) spessartite, rhodochrosite, and quartz, ± hematite, ± chamosite; (3) rhodochrosite, spessartite, pyroxmanite, quartz ± tephroite, ± fridelite, ± clinochlore, ± pyrophanite, ± pyrite. In all varieties, the major concentrators of Mn and Fe are carbonates (rhodochrosite, siderite, kutnahorite, Mn-calcite) and chlorite group minerals (clinochlore, chamosite). The chemical composition of rocks is dominated by Si, Fe, Mn, carbon dioxide, and water (L.O.I.): total SiO2 + Fe2O 3 tot + MnO + L.O.I. = 85.6?98.4 wt %. The content of Fe and Mn varies from 9.3 to 55.6 wt % (Fe2O 3 tot + MnO). The Mn/Fe ratio varies from 0.2 to 55.3. In terms of the aluminum module AlM = Al/(Al + Mn + Fe), the major portion of studied samples corresponds to metalliferous sediments. The δ13Ccarb range (–30.4 to–11.9‰ PDB) corresponds to authigenic carbonates formed with carbon dioxide released during the microbial oxidation of organic matter in sediments at the dia- and/or catagenetic stage. Ferromanganese sediments were likely deposited in relatively closed seafloor zones (basin-traps) characterized by periodic stagnation. Fe and Mn could be delivered from various sources: input by diverse hydrothermal solutions, silt waters in the course of diagenesis, river discharges, and others. The diagenetic delivery of metals seems to be most plausible. Mn was concentrated during the stagnation of bottom water in basin-traps. Interruption of stagnation promoted the precipitation of Mn. The presence of organic matter fostered a reductive pattern of postsedimentary transformations of metalliferous sediments. Fe and Mn were accumulated initially in the oxide form. During the diagenesis, manganese and iron oxides reacted with organic matter to make up carbonates. Relative to manganese carbonates, iron carbonates were formed under more reductive settings and higher concentrations of carbon dioxide in the interstitial solution. Crystallization of manganese and iron silicates began already at early stages of lithogenesis and ended during the regional metamorphism of metalliferous sediments. 相似文献