成矿作用过程中赤铁矿—磁铁矿之间非氧化还原转变

自然界中铁氧化物的主要存在形式为赤铁矿和磁铁矿,两者之间的相互转变一直是人们关注和研究的热点。磁铁矿和赤铁矿之间的相互转变一直被认为是一个氧化还原反应的结果,反应的发生与一定的氧化剂或还原剂密切相关。然而,近年来一个铁氧化物之间的非氧化还原反应机制被提出,这种非氧化还原反应机制对于认识和了解复杂的成矿作用具有重要的意义。本文阐述了自然界中铁氧化物之间的相互交代结构,对BIF研究和实验学两方面的证据进行了综述,认为这种非氧化还原反应可能存在于很多不同类型的成矿作用过程之中。这种赤铁矿和磁铁矿之间的非氧化还原反应机制具有重要的理论和实际意义:一方面,仅靠地质作用过程中出现磁铁矿或赤铁矿现象不一定就能判别其形成流体的氧化还原状态;另一方面,它可以为勘探含后生赤铁矿的铁矿床提供新的找矿思路,进一步指导深埋在古风化面以下铁矿体的寻找。     

Gold Mineralization in Banded Iron Formation in the Amalia Greenstone Belt,South Africa: A Mineralogical and Sulfur Isotope Study

The Blue Dot gold deposit, located in the Archean Amalia greenstone belt of South Africa, is hosted in an oxide (± carbonate) facies banded iron formation (BIF). It consists of three stratabound orebodies; Goudplaats, Abelskop, and Bothmasrust. The orebodies are flanked by quartz‐chlorite‐ferroan dolomite‐albite schist in the hanging wall and mafic (volcanic) schists in the footwall. Alteration minerals associated with the main hydrothermal stage in the BIF are dominated by quartz, ankerite‐dolomite series, siderite, chlorite, muscovite, sericite, hematite, pyrite, and minor amounts of chalcopyrite and arsenopyrite. This study investigates the characteristics of gold mineralization in the Amalia BIF based on ore textures, mineral‐chemical data and sulfur isotope analysis. Gold mineralization of the Blue Dot deposit is associated with quartz‐carbonate veins that crosscut the BIF layering. In contrast to previous works, petrographic evidence suggests that the gold mineralization is not solely attributed to replacement reactions between ore fluid and the magnetite or hematite in the host BIF because coarse hydrothermal pyrite grains do not show mutual replacement textures of the oxide minerals. Rather, the parallel‐bedded and generally chert‐hosted pyrites are in sharp contact with re‐crystallized euhedral to subhedral magnetite ± hematite grains, and the nature of their coexistence suggests that pyrite (and gold) precipitation was contemporaneous with magnetite–hematite re‐crystallization. The Fe/(Fe+Mg) ratio of the dolomite–ankerite series and chlorite decreased from veins through mineralized BIF and non‐mineralized BIF, in contrast to most Archean BIF‐hosted gold deposits. This is interpreted to be due to the effect of a high sulfur activity and increase in fO₂ in a H₂S‐dominant fluid during progressive fluid‐rock interaction. High sulfur activity of the hydrothermal fluid fixed pyrite in the BIF by consuming Fe²⁺ released into the chert layers and leaving the co‐precipitating carbonates and chlorites with less available ferrous iron content. Alternatively, the occurrence of hematite in the alteration assemblage of the host BIF caused a structural limitation in the assignment of Fe³⁺ in chlorite which favored the incorporation of magnesium (rather than ferric iron) in chlorite under increasing fO₂ conditions, and is consistent with deposits hosted in hematite‐bearing rocks. The combined effects of reduction in sulfur contents due to sulfide precipitation and increasing fO₂ during progressive fluid‐rock interactions are likely to be the principal factors to have caused gold deposition. Arsenopyrite–pyrite geothermometry indicated a temperature range of 300–350°C for the associated gold mineralization. The estimated δ³⁴S_ΣS (= +1.8 to +2.5‰) and low base metal contents of the sulfide ore mineralogy are consistent with sulfides that have been sourced from magma or derived by the dissolution of magmatic sulfides from volcanic rocks during fluid migration.     

Mechanism and kinetics of hydrothermal replacement of magnetite by hematite

The replacement of magnetite by hematite was studied through a series of experiments under mild hydrothermal conditions(140 -220℃, vapour saturated pressures) to quantify the kinetics of the transformation and the relative effects of redox and non-redox processes on the transformation. The results indicate that oxygen is not an essential factor in the replacement reaction of magnetite by hematite, but the addition of excess oxidant does trigger the oxidation reaction, and increases the kinetics of the transformation. However, even under high O_2(aq) environments, some of the replacement still occurred via Fe²⁺ leaching from magnetite. The kinetics of the replacement reaction depends upon temperature and solution parameters such as pH and the concentrations of ligands, all of which are factors that control the solubility of magnetite and affect the transport of Fe²⁺ (and the oxidant) to and from the reaction front. Reaction rates are fast at ~200℃, and in nature transport properties of Fe and,in the case of the redox-controlled replacement, the oxidant will be the rate-limiting control on the reaction progress. Using an Avrami treatment of the kinetic data and the Arrhenius equation, the activation energy for the transformation under non-redox conditions was calculated to be 26 ± 6 kJ mol^-1.This value is in agreement with the reported activation energy for the dissolution of magnetite, which is the rate-limiting process for the transformation under non-redox conditions.     

BIF-hosted iron mineral system: A review

The BIF-hosted iron ore system represents the world's largest and highest grade iron ore districts and deposits. BIF, the precursor to low- and high-grade BIF hosted iron ore, consists of Archean and Paleoproterozoic Algoma-type BIF (e.g., Serra Norte iron ore district in the Carajás Mineral Province), Proterozoic Lake Superior-type BIF (e.g., deposits in the Hamersley Province and craton), and Neoproterozoic Rapitan-type BIF (e.g., the Urucum iron ore district).The BIF-hosted iron ore system is structurally controlled, mostly via km-scale normal and strike-slips fault systems, which allow large volumes of ascending and descending hydrothermal fluids to circulate during Archean or Proterozoic deformation or early extensional events. Structures are also (passively) accessed via downward flowing supergene fluids during Cenozoic times.At the depositional site the transformation of BIF to low- and high-grade iron ore is controlled by: (1) structural permeability, (2) hypogene alteration caused by ascending deep fluids (largely magmatic or basinal brines), and descending ancient meteoric water, and (3) supergene enrichment via weathering processes. Hematite- and magnetite-based iron ores include a combination of microplaty hematite–martite, microplaty hematite with little or no goethite, martite–goethite, granoblastic hematite, specular hematite and magnetite, magnetite–martite, magnetite-specular hematite and magnetite–amphibole, respectively. Goethite ores with variable amounts of hematite and magnetite are mainly encountered in the weathering zone.In most large deposits, three major hypogene and one supergene ore stages are observed: (1) silica leaching and formation of magnetite and locally carbonate, (2) oxidation of magnetite to hematite (martitisation), further dissolution of quartz and formation of carbonate, (3) further martitisation, replacement of Fe silicates by hematite, new microplaty hematite and specular hematite formation and dissolution of carbonates, and (4) replacement of magnetite and any remaining carbonate by goethite and magnetite and formation of fibrous quartz and clay minerals.Hypogene alteration of BIF and surrounding country rocks is characterised by: (1) changes in the oxide mineralogy and textures, (2) development of distinct vertical and lateral distal, intermediate and proximal alteration zones defined by distinct oxide–silicate–carbonate assemblages, and (3) mass negative reactions such as de-silicification and de-carbonatisation, which significantly increase the porosity of high-grade iron ore, or lead to volume reduction by textural collapse or layer-compaction. Supergene alteration, up to depths of 200 m, is characterised by leaching of hypogene silica and carbonates, and dissolution precipitation of the iron oxyhydroxides.Carbonates in ore stages 2 and 3 are sourced from external fluids with respect to BIF. In the case of basin-related deposits, carbon is interpreted to be derived from deposits underlying carbonate sequences, whereas in the case of greenstone belt deposits carbonate is interpreted to be of magmatic origin. There is only limited mass balance analyses conducted, but those provide evidence for variable mobilization of Fe and depletion of SiO₂. In the high-grade ore zone a volume reduction of up to 25% is observed.Mass balance calculations for proximal alteration zones in mafic wall rocks relative to least altered examples at Beebyn display enrichment in LOI, F, MgO, Ni, Fe₂O_3total, C, Zn, Cr and P₂O₅ and depletions of CaO, S, K₂O, Rb, Ba, Sr and Na₂O. The Y/Ho and Sm/Yb ratios of mineralised BIF at Windarling and Koolyanobbing reflect distinct carbonate generations derived from substantial fluid–rock reactions between hydrothermal fluids and igneous country rocks, and a chemical carbonate-inheritance preserved in supergene goethite.Hypogene and supergene fluids are paramount for the formation of high-grade BIF-hosted iron ore because of the enormous amount of: (1) warm (100–200 °C) silica-undersaturated alkaline fluids necessary to dissolve quartz in BIF, (2) oxidized fluids that cause the oxidation of magnetite to hematite, (3) weakly acid (with moderate CO₂ content) to alkaline fluids that are necessary to form widespread metasomatic carbonate, (4) carbonate-undersaturated fluids that dissolve the diagenetic and metasomatic carbonates, and (5) oxidized fluids to form hematite species in the hypogene- and supergene-enriched zone and hydroxides in the supergene zone.Four discrete end-member models for Archean and Proterozoic hypogene and supergene-only BIF hosted iron ore are proposed: (1) granite–greenstone belt hosted, strike-slip fault zone controlled Carajás-type model, sourced by early magmatic (± metamorphic) fluids and ancient “warm” meteoric water; (2) sedimentary basin, normal fault zone controlled Hamersley-type model, sourced by early basinal (± evaporitic) brines and ancient “warm” meteoric water. A variation of the latter is the metamorphosed basin model, where BIF (ore) is significantly metamorphosed and deformed during distinct orogenic events (e.g., deposits in the Quadrilátero Ferrífero and Simandou Range). It is during the orogenic event that the upgrade of BIF to medium- and high-grade hypogene iron took place; (3) sedimentary basin hosted, early graben structure controlled Urucum-type model, where glaciomarine BIF and subsequent diagenesis to very low-grade metamorphism is responsible for variable gangue leaching and hematite mineralisation. All of these hypogene iron ore models do not preclude a stage of supergene modification, including iron hydroxide mineralisation, phosphorous, and additional gangue leaching during substantial weathering in ancient or Recent times; and (4) supergene enriched BIF Capanema-type model, which comprises goethitic iron ore deposits with no evidence for deep hypogene roots. A variation of this model is ancient supergene iron ores of the Sishen-type, where blocks of BIF slumped into underlying karstic carbonate units and subsequently experienced Fe upgrade during deep lateritic weathering.     

Ore petrology of the V-Ti magnetite (lodestone) layers of the Kurihundi area of Sargur schist belt,Dharwar craton

The V-Ti magnetite layers (lodestone) occur within the layered gabbro-anorthosites-ultramafic rocks emplaced into the migmatitic gneisses close to the high grade Archeaen Sargur supracrustal rocks in the Kurihundi area. The ore petrographic studies of the lodestone reveal the presence of primary Ti-magnetite, ilmenite, ulvospinel, pleonaste, hematite and pyrite, chalcopyrite, pyrrhotite and secondary Ti-maghemite, martite and goethite as well as secondary covellite. These layers contain Ti-magnetite (60%) and ilmenite (30%) with silicates (<5%) exhibiting granular mosaic texture with well-defined triple junctions and are classified as adcumulus rocks. The grain-boundary relationships in the ores indicate considerable postcumulus growth and readjustment due to combined effects of sintering and adcumulus growth. Intergrowth textures (ulvospinel, ilmenite and pleonaste in Ti-magnetite and hematite in ilmenite) reflects exsolution features crystallized from solid-solutions compositions under different conditions of oxygen fugacities. Larger bodies of pleonaste and ilmenite in Ti-magnetite become lensoid or rounded in outline and these morphological modifications took place during the regional upper amphibolite to lower granulite facies metamorphism at 2.6 Ga ago. The lodestone contains high TiO₂ (20 to 22.59 wt%), with V₂O₅ (0.85 to 1.15%) and Fe₂O₃ ^t (72.03 to 74.25%). Ti-magnetite shows alteration to Ti-maghemite, martite and goethite due to low temperature oxidation and hydration during weathering.     

Ferruginous and manganiferous haloes around massive sulphide deposits of the Urals

Proximal brecciform ferruginous and manganiferous rocks related to VMS deposits of the Urals are subdivided into jasperites, gossanites, and umbers, in addition to thin-bedded jaspers and cherts. The coherence of host rock composition and Mn–Fe-fertility of the sediments have been established. Fe-poor pink hematitic and gray sulphidic chert are typical of the felsic class of VMS deposits. In contrast the contents of Fe vary from high to moderate in ferruginous rocks enclosed in basaltic units associate with VMS deposits. Fe- and Mn-rich ferruginous rocks and umbers occur in association with limestones and calcareous sedimentary rocks in both types of volcanic sequences. A common feature of jasperites and umbers is the abundance of replacement textures of hyaloclastites and carbonates by hematite and silica. In addition, replacement of clastic sulphides by hematite and magnetite is a characteristic genetic feature of gossanites. All of these sedimentary rocks are accompanied by pseudomorphs of hematite and quartz formed after bacterial filaments. The abundance of replacement textures are supportive of the halmyrolysis model, in addition to hydrothermal sedimentary and sub-seafloor hydrothermal replacement theories. Study of chemical zonation of altered hyaloclasts shows depletion of their rims, not only in mobile Na, K, Mg, but also in immobile Al, Ti, and REE; whereas Si and Fe are concentrated in situ. The halmyrolysis model presented here, involving organic-rich calcareous hyaloclastic sediments, resolves the problem of subtraction of Al, Ti, REE and other elements, which are commonly immobile under hydrothermal conditions. The evolution of the halmyrolysis process from acidic reducing to alkaline oxidized conditions infers a possible range in transformation from Fe^II–Mg smectites to Fe-silicates and Fe-Si oxides as precursors of brecciform jasperite and thin-bedded jasper. The higher acidic, initial stage, of gossanite formation seems to be required for oxidation of organic matter and/or pyrite. The acidic condition facilitates the temporal preservation of “immobile” elements (Al, Ti, REE) in “immature”chlorite–hematite gossanites. Another peculiarity of the gossanite-forming processes is the likely sorption of P, U and V by iron hydroxides displacing sulphides. The general evolution of all ferruginous sediments results in complete Fe²⁺ oxidation and silicification accompanied by subtraction of other elements. The vertical diagenetic differentiation leads to concentration of Mn-carbonates, silicates and oxyhydroxides into the tops of jasperite and gossanite layers. Mn oxyhydroxides scavenge positively charged hydrated cations like Co and Ni. Near-vent bacterial communities may activate the processes of volcanic glass and sulphide degradation. The proposed processes of halmyrolysis followed by silicification, in situ, may resolve the enigma of silica-rich sediment formation in a silica undersaturated ocean. The discrimination between gossanite and jasperite is useful for elaboration of new criteria for local exploration of VMS- and Mn-deposits. Halo dispersion of gossanites covering an area about two to three times that of the massive sulphide deposit is a good vector for ore body discovery. Proximal gossanites can be differentiated from jasperites by presence of relic sulphide clasts or elevated contents of chalcophile elements (Cu, Fe, Zn, Pb, Bi, Te, As, Sb, Ba), noble metals (Au, Ag) and distinct REE patterns with La and Eu positive anomalies. The development of halmyrolysis and biomineralization models merit further elaboration and testing in on-going research, in order to add or revise theories of iron and manganese deposit formation.     

Geological,mineralogical, and oxygen isotope studies of the Chandmani Uul iron oxide–copper–gold deposit in Dornogobi Province,Southeastern Mongolia

The Chandmani Uul deposit is located in Dornogovi province, Southeastern Mongolia. Iron oxide ores are hosted in the andesitic rocks of the Shar Zeeg Formation of Neoproterozoic to Lower‐Cambrian age. Middle‐ to Upper‐Cambrian bodies of granitic rocks have intruded into the host rocks in the western and southern regions of the deposit. The wall rocks around the iron oxide ore bodies were hydrothermally altered to form potassic, epidote, and sericite–chlorite alteration zones, and calcite and quartz veinlets are ubiquitous in the late stage. Since granitic rocks also underwent potassic alteration, the activity of the granitic rocks must have a genetic relation to the ore deposit. The ore mineral assemblage is dominated by iron oxides such as mushketovite, euhedral magnetite with concentric and/or oscillatory zoning textures, and cauliflower magnetite. Lesser amounts of chalcopyrite and pyrite accompany the iron oxides. Among all these products, mushketovite is dominant and is distributed throughout the deposit. Meanwhile, euhedral magnetite appears in limited amounts at relatively shallow levels in the deposit. By contrast, cauliflower magnetite appears locally in the deeper parts of the deposit, and is associated with green‐colored garnet and calcite. Sulfide minerals are ubiquitously associated with these iron oxides. The oxygen isotope (δ¹⁸O) values of all types of magnetite, quartz, and epidote were found to be ?5.9 to ?2.8‰, 10.5 to 14.9‰, and 3.6 to 6.6‰, respectively. The δ¹⁸O values of quartz–magnetite pairs suggest an equilibrium isotopic temperature near 300°C. The calculated values of δ¹⁸O for the water responsible for magnetite ranged from 2 to 10‰. All the data obtained in this study suggest that the iron oxide deposit at the Chandmani Uul is a typical iron oxide–copper–gold deposit, and that this deposit was formed at an intermediate depth with potassic and sericite–chlorite alteration zones under the oxidized conditions of a hematite‐stable environment. The δ¹⁸O range estimated implies that the ore‐forming fluid was supplied by a crystallizing granodioritic magma exsolving fluids at depth with a significant contribution of meteoric water.     

Micro- to nano-scale characterization of martite from a banded iron formation in India and a lateritic soil in Brazil

The pseudomorphic transformation of magnetite into hematite (martitization) is widespread in geological environments, but the process and mechanism of this transformation is still not fully understood. Micro- and nano-scale techniques—scanning electron microscopy, focused ion bean transmission electron microscopy, and Raman spectroscopy—were used in combination with X-ray diffraction, Curie balance and magnetic hysteresis analyses, as well as Mössbauer spectroscopy on martite samples from a banded iron formation (2.9 Ga, Dharwar Craton, India), and from lateritic soils, which have developed on siliciclastic and volcanic rocks previously affected by metamorphic fluids (Minas Gerais, Brazil). Octahedral crystals from both samples are composed of hematite with minor patches of magnetite, but show different structures. The Indian crystals show trellis of subhedral magnetite hosting maghemite in sharp contact with interstitial hematite crystals, which suggests exsolution along parting planes. Grain boundary migrations within the hematite point to dynamic crystallization during deformation. Dislocations and fluid inclusions in hematite reflect its precipitation related to a hydrothermal event. In the Brazilian martite, dislocations are observed and maghemite occurs as Insel structures and nano-twin sets. The latter, typical for the hematite, are a transformation product from maghemite into hematite. For both samples, a deformation-induced hydrothermally driven transformation from magnetite via maghemite to hematite is proposed. The transformation from magnetite into maghemite comprises intermediate non-stoichiometric magnetite steps related to a redox process. This study shows that martite found in supergene environment may result from earlier hypogene processes.     

Oxide and sulphide isograds along a Late Archean, deep-crustal profile in Tamil Nadu, south India

Oxide–sulphide–Fe–Mg–silicate and titanite–ilmenite textures as well as their mineral compositions have been studied in felsic and intermediate orthogneisses across an amphibolite (north) to granulite facies (south) traverse of lower Archean crust, Tamil Nadu, south India. Titanite is limited to the amphibolite facies terrane where it rims ilmenite or occurs as independent grains. Pyrite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade. Pyrrhotite is confined to the high‐grade granulites. Ilmenite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade and occurring primarily as hemo‐ilmenite in the high‐grade granulite facies rocks. Magnetite is widespread throughout the traverse and is commonly associated with ilmenite. It decreases in abundance with increasing metamorphic grade. In the granulite facies zone, reaction rims of magnetite + quartz occur along Fe–Mg silicate grain boundaries. Magnetite also commonly rims or is associated with pyrite. Both types of reaction rims represent an oxidation effect resulting from the partial subsolidus reduction of the hematite component in ilmenite to magnetite. This is confirmed by the presence of composite three oxide grains consisting of hematite, magnetite and ilmenite. Magnetite and magnetite–pyrite micro‐veins along silicate grain boundaries formed over a wide range of post‐peak metamorphic temperatures and pressures ranging from high‐grade SO₂ to low‐grade H₂S‐dominated conditions. Oxygen fugacities estimated from the orthopyroxene–magnetite–quartz, orthopyroxene–hematite–quartz, and magnetite–hematite buffers average 2.5 log units above QFM. It is proposed that the trends in mineral assemblages, textures and composition are the result of an external, infiltrating concentrated brine containing an oxidizing component such as CaSO₄ during high‐grade metamorphism later acted upon by prograde and retrograde mineral reactions that do not involve an externally derived fluid phase.     

Magnetite, ilmenite and ulvite in rocks and ore deposits: petrography, microprobe analyses and genetic implications

Summary ?Detailed petrographic studies and microchemical analyses of titanomagnetite from igneous and metamorphic rocks and ore deposits form the basis of this investigation. Its aim is to compare the data obtained and their interpretations with the experimentally deduced subsolidus oxidation-exsolution model of Buddington and Lindsley (1964). The results are also considered relevant for the interpretation of compositional variations in black sands which are recovered for titanium production. The arrangement of the samples investigated is in accordance with textural stages C1 to C5 caused by subsolidus exsolution with increasing degrees of oxidation (Haggerty, 1991). Stage 1 is represented by two types of optically homogeneous TiO₂-rich magnetite: a. An isotropic type considered to represent solid solutions of magnetite and ulvite containing between 5.2 to 27.5 wt% TiO₂ corresponding to about 14.7 to 77.7 mol% Fe₂TiO₄ in solid solution with magnetite. The general formula of this type is Fe²⁺ _1+x Fe³⁺ _2−2x Ti _x O₄ (x = 0.0–1.0). b. The second type which has not been reported so far is anisotropic and shows complex internal twinning resembling inversion textures. It is thus attributed to inversion of a high-temperature ilmenite modification (with statistical distribution of the cations) which forms solid solutions with magnetite. TiO₂ varies between 9.3 and 24.5 wt% corresponding to about 17.2 to 43.6 mol% ilmenite in solid solution with magnetite. This type is interpreted as a cation-deficient spinel with the general formula Fe²⁺ _{12/12 + 1/4x}Fe³⁺ _{24/12 − 3/2x} □ _{0 + 1/4x} Ti _x O₄ (x = 0.0–16/12). Isotropic and anisotropic homogeneous magnetites occur in volcanic rocks only; the homogeneity of the solid solutions was explained by fast cooling which prevented the development of exsolution textures. Stages 2 and 3 are represented by magnetite with or without ulvite. The magnetite host contains ilmenite lamellae forming trellis and sandwich textures. In contrast to the requirement of the oxidation-exsolution model, the ilmenite lamellae are concentrated exclusively in the cores of the host crystals. The reverse host-guest relationship may also occur. Stages 4 and 5 are identical with thermally generated martite (= martite due to heating). The textures are characterized by very broad lamellae of ferrian ilmenite or titanohematite dominantly concentrated along the margins of the host crystals. Thermally generated martite is restricted to subsolidus-oxidation reactions. The ilmenite lamellae of trellis and sandwich textures contain low Fe₂O₃-concentrations (average 4.8 mol%; to a maximum of 8.3), whereas the Fe₂O₃-content of thermally generated martite is between 32 to 71 mol%. With respect to the Fe₂O₃-concentrations in the ilmenite lamellae, no transition between the two types was observed. The results of this paper show that the widely accepted oxy-exsolution model of Buddington and Lindsley (1964) which is based on experimental results can – with the exception of thermally generated martite – not explain the tremendous variety of magnetite–ilmenite–ulvite relationships in natural rocks and ore deposits. Received October 16, 2001; accepted May 2, 2002     

繁昌桃冲铁矿成因探讨

The problems of the formation conditions for stratiform skarns and the genesis of the Taochong iron deposits are dealt with in this paper. Following is a summary of this discussion: 1. Stratiform skarns in this area occur in carbonate rocks of the Upper and Middle Carboniferous Period and the lower part of the Permian Qixia Group. No outcropping or concealed igneous bodies have ever been found, let alone any indications of an igneous contact zone or a corresponding zonality from "dry" skarn to "wet" skarn. The mineral facies and zonation of the skarns depend predominantly on the properties of the initial host rocks, and the development of skarns seems to have had much to do with chemical potential of silicon in these host rocks. As a result of the reaction of iron-bearing carbonates with siliceous materials in the rocks, iron-bearing silicates were formed, which in turn were transformed by pneumato-hydrothermal processes of the later stage. The stratiform skarns of this area, therefore, probably fall into the category of stratabound skarns subjected to transformation of thermometamorphism. 2. The iron deposits bear undisputable stratabound characteristics. The positions of ore-bearing beds and the petrological features as well as the mineral associations all point to a sedimentary ore-forming process of iron-carbonate (siderite). The presumption of siderite ore source is supported by the following facts: (l) Remnants of sedimentary siderite which survived the metamorphism have recently been observed in magnetite ore from neighbouring Xinqiao mining area. Siderite can have as many as 12.07% Fe⁺⁺ and, after corrosion, shows oolitic texture. (2) The ore is mainly of calcite/ dolomite- magnetite type. Mineral associations are quite simple and sulfides are rarely seen. (3) A comparison of the analytical data suggests that the content of organic carbon in iron ore decreases due to oxidation caused by metamorphism but is still higher than that in magnetite of contact- metasomatic skarn. (4) The paleogeographic reconstruction shows that this area was once an ancient underwater uplift favorable for the precipitation of iron carbonates. After its formation, the siderate bed underwent thermodynamic metamorphism and was hence decomposed into magnetite, which was then subjected to the superimposed transformation by subsequent hydrothermal fluids, leading to the partial activation and migration of iron matter and thus the formation of such ore as hematite (specularite) at shallow depth of the Changlongshan mining area. In brief, this deposit has a complex genesis: it experienced sedimentation, thermal metamorphism and transformation by hydrothermal fluids.     

繁昌桃冲铁矿成因探讨

桃冲铁矿,开采历史悠久,由于其品位富,以平炉富矿为主要矿石类型,受到了重视。有关矿床的成因也一直被人们所注意。自三十年代提出火成接触变质——热液成因的观点以来(谢家荣、程裕淇1935),人们习惯于将矿床划归于矽卡岩型。作者通过野外调查和初步研究之后,对本区铁矿的成因产生了疑问。本文就现有资料的分析,对层状矽卡岩的形成条件和铁矿的成因,做如下讨论。     

Mineralogy and Petrology of the Gunflint Iron Formation, Minnesota-Ontario: Correlation of Compositional and Assemblage Variations at Low to Moderate Grade

Near the Ontario—Minnesota boundary, the middle Precambriansedimentary Gunflint Iron Formation has been contact metamorphosedby the Duluth Complex to the pyroxene hornfels facies. Threemetamorphic zones have been recognized based on mineralogicalchanges observed within the aureole; a fourth zone correspondsto essentially unmetamorphosed iron formation. Each zone maybe recognized by the dominant iron silicate present: zone 1—greenalitezone (unmetamorphosed), zone 2—minnesotaite zone (slightlymetamorphosed), zone 3—grunerite zone (moderately metamorphosed),zone4—ferrohypersthene zone (highly metamorphosed). Granule bearing cherty rocks of zone 2 are characterized bythe reduction of hematite to magnetite and reaction of greenaliteand siderite to minnesotaite ± magnetite. Relict texturesare well preserved in zone 2 and retrograde reactions are minimal.Grunerite first appears in banded slaty rocks of zone 3. ‘Slaty’grunerite formed principally by reaction between carbonate andstilpnomelane, while in cherty rocks grunerite formed by reactionbetween greenalite and silica. Original bulk chemical differencesbetween cherty and slaty iron formation is reflected by amphibolechemistry as shown by the higher Al content and lower Fe/Fe+ Mg ratio of slaty grunerite, and by the greater ahundanceof Na, Al-bearing amphiboles such as ferrotschermakite in slatyrocks. Hedenbergite and fayalite appear in the upper part ofzone 3; both formed by silication of carbonates and both arepartially retrograded to amphibole. Prograde grunerite-cummingtoniteis partially replaced by minnesotaite in cherty rocks of zones3 and 4. In zone 4, greenalite and siderite-bearing assemblagesreacted to ferrohypersthene, fayalite (±quartz), pigeoniteand grunerite-cummingtonite. Retrogradation is widespread andresulted mainly in the formation of grunerite. Primary textureswere destroyed in slaty rocks but are still recognizable incherty rocks. Preservation of sedimentary textures within the contact aureoleis a characteristic feature of cherty rocks. In zone l theserocks typically consist of the following textural-mineralogicalassociation: granules (greenalite, quartz, hematite), cement(quartz, siderite, ankerite, calcite) and mottles (various carbonates).Retention of these textural elements, combined with compositionaldata for assemblages in the low to moderate grade rocks, enablesidentification of numerous metamorphic reactions. In the absenceof relict phases or relict textures sedimentary assemblagescan sometimes be inferred from abundances of minor elementssuch as Al and Mn. In some slaty rocks the presence of carbonaceous or graphiticmaterial has preserved perfectly premetamorphic structures suchas siderite spherules and ankerite rhombs, enabling the recognitionof several amphibole-forming reactions. Chemographic analysis of simplified subsystems for cherty rocksof zone 1, zone 2, and the lower part of zone 3, are consistentwith observed assemblages and reactions.     

Phase equilibria in rocks of the paleoproterozoic banded iron formation (BIF) of the Lebedinskoe deposit, Kursk Magnetic Anomaly, and the petrogenesis of BIF with alkali amphiboles

BIF with alkali amphibole at the Lebedinskoe iron deposits, the largest in Russia, were metamorphosed at 550°C and 2–3 kbar and contain ferriwinchite, riebeckite, actinolite, grunerite, and aegirine-augite. All reaction textures observed in the rocks were produced during the prograde metamorphic stage and represent the following succession of mineral replacements: Gru → Rbk, Act → Win → Rbk. Data obtained on the textural relations and compositional variations of Ca, Ca-Na, and Na Al-free amphiboles point to the complete miscibility in the actinolite-ferriwinchite and ferriwinchite-riebeckite isomorphic series. Riebeckite is formed in BIF during the prograde metamorphic stage, with the participation of a fluid insignificantly enriched in Na⁺ and at increasing oxygen fugacity. The critical factors controlling the development of alkali amphiboles and Ca-Na pyroxenes in carbonate-bearing BIF is the oxygen activity and the presence of at least low concentrations of Na⁺ ions in the fluid. The minerals contain Fe³⁺, and all reactions producing them are oxidation reactions. The origin of riebeckite late in the course of the mineral-forming process is caused by the Ca²⁺Mg²⁺ → Na⁺Fe³⁺ heterovalent isomorphic replacement in calcic and calcic-sodic amphiboles and by the oxidation of grunerite in the presence of a fluid enriched in Na ions.     

神农架式铁矿特征简介

神农架铁矿位于华中第一高峰——鄂西神农架原始林区。目前发现具有工业价值的矿区主要有两个:一个在铁厂河,另一个在大神农架主峰附近(图1)。铁矿露头一般在标高2000—2500米以上。虽然该铁矿沉积形成于元古代,但由于它至今几乎未受变质,使它具有独特的矿石类型,以区别于一般前寒武纪沉积变质铁矿,因此人们专称它为神农架式。现将该铁矿特征简要报道如下。     

Geology of the Gushan iron oxide deposit associated with dioritic porphyries,eastern Yangtze craton,SE China

The major Gushan iron oxide deposit, typical of the Middle‐Lower Yangtze River Valley, is located in the eastern Yangtze craton. Such deposits are generally considered to be genetically related to Yanshanian subvolcanic‐volcanic rocks and are temporally‐spatially associated with ca. 129.3–137.5 Ma dioritic porphyries. The latter have a very narrow ⁸⁷Sr/⁸⁶Sr range of 0.7064 to 0.7066 and low ?_Nd(t) values of ?5.8 to ?5.7, suggesting that the porphyries were produced by mantle‐derived magmas that were crustally contaminated during magma ascent. The ore bodies occur mainly along the contact zone between dioritic porphyries and the sedimentary country rocks. The most important ore types are massive and brecciated ores which together make up 90 vol.‐% of the deposit. The massive type generally occurs as large veins consisting predominantly of magnetite (hematite) with minor apatite. The brecciated type is characterized by angular fragments of wall‐rocks that are cemented by fine‐grained magnetite. Stockwork iron ores occur as irregular veins and networks, especially with pectinate structure; they are composed of low‐temperature minerals (e.g. calcite), which indicate a hydrothermal process. The similar rare earth element patterns of apatite from the massive ores, brecciated ores and the porphyries, coupled with high‐temperature fluids (1000°C) suggest that they are magmatic in origin. Furthermore, melt flow structure commonly developed in massive ores and the absence of silicate minerals and cumulate textures suggest that the iron ores formed by the separation of an immiscible oxide melt from the silicate melt rather than by crystal fractionation. Combined with theoretical and experimental studies, we propose that the introduction of phosphorus due to crustal contamination during mantle‐derived magma ascent could have been a crucial factor that led to the formation of an immiscible oxide melt from the silicate magma.     

新疆西天山松湖铁矿床稀土和微量元素地球化学特征及其意义

松湖铁矿床位于新疆西天山阿吾拉勒成矿带中段,赋存于石炭系大哈拉军山组火山-沉积岩系中。矿体呈似层状、透镜状,主要受近EW向、NWW向高角度逆断层控制。矿石主要呈块状、条带状、团块状构造,结构主要为半自形-他形粒状;矿石矿物主要为磁铁矿,其次为赤铁矿、黄铁矿及黄铜矿,脉石矿物主要为钾长石、绿泥石、方解石、绿帘石及阳起石等。围岩蚀变发育,在垂向和水平方向上具有分带性。矿区围岩是阿吾拉勒地区早石炭世岛弧火山岩的组成部分,不同岩性具有类似的稀土元素配分模式,均为轻稀土元素富集的右倾型,发育弱的负铈异常,中到弱的负铕或正铕异常。矿石中磁铁矿的∑REE值变化于20.75×10-6~65.41×10-6,配分模式为轻稀土元素富集的右倾型,发育中到弱的负铈及负铕异常。磁铁矿与围岩的稀土元素特征表明二者具有成因联系,与岛弧火山作用有关。磁铁矿微量元素特征表明成矿物质来源于深部,磁铁矿为火山热液交代成因。结合矿床地质特征,认为松湖铁矿床为海相火山热液型矿床。     

Diagenetic crystallization and oxidation of siderite in red bed (Buntsandstein) sediments from the Central Iberian Chain,Spain

Compactional deformation facilitated replacement of dolomite and calcite by siderite and its subsequent oxidation in carbonate cemented red beds of the Triassic Buntsandstein in the Iberian Chain. Locally, the sedimentary clasts were cemented by carbonate that was derived from dissolution of locally exposed dolomite in the basement. Microstructures indicate that during sedimentation of the rocks, oxidizing conditions prevailed in the sediments and the basement was reddened by impregnation of hematite. Reducing conditions prevailed during deformation of the sediments. Ferric iron was reduced to Fe²⁺, that reacted with deformed dolomite and calcite cement to produce fine grained siderite. At a later stage, siderite crystallites were (partly) oxidized to form a secondary phase of brown ferric oxide (goethite). Locally, goethite transformed to fine grained hematite that caused secondary reddening of the sediments. The reactions are associated with a combined volume loss of the solid phases of c. 50% per reaction mol; this was accommodated by the formation of pores. Oxidation of siderite was associated with release of CO₂; localized dissolution took place of feldspar and concurrently growth of kaolinite occurred by acidifying condition during release of CO₂. The relation of redox reactions and deformation is comparable to those in red bed conglomerates in the region. Reductive dissolution occurred at sites of stress concentration, particularly at contact points of pebbles. Late stage precipitation of ferric oxides and pyrolusite took place at oxidizing conditions in association with uplift.     

Fe–Cu deposits in the Kangdian region,SW China: a Proterozoic IOCG (iron-oxide–copper–gold) metallogenic province

Numerous Fe–Cu deposits are hosted in the late Paleoproterozoic Dongchuan and Dahongshan Groups in the Kangdian region, SW China. The Dongchuan Group is composed of siltstone, slate, and dolostone with minor volcanic rocks, whereas the Dahongshan Group has undergone lower amphibolite facies metamorphism and consists of quartz mica-schist, albitite, quartzite, marble and amphibolite with local migmatite. Deposits in the Dongchuan Group are commonly localized in the cores of anticlines, in fault bends and intersections, and at lithological contacts. Orebodies are closely associated with breccias, which are locally derived from the host rocks. Fe-oxides (magnetite and/or hematite) and Cu-sulfides (chalcopyrite, bornite) form disseminated, vein-like and massive ores, and typically fill open spaces in the host rocks. The deposits have extensive albite alteration and local K-feldspar alteration overprinted by quartz, carbonate, sericite and chlorite. Deposits in the Dahongshan Group have orebodies sub-parellel to stratification and show crude stratal partitioning of metals. Fe-oxide ores occur as massive and/or banded replacements within the breccia pipes, whereas Cu-sulfide ores occur predominantly as disseminations and veinlets within mica schists and massive magnetite ores. Ore textures suggest that Cu-sulfides formed somewhat later than Fe-oxides, but are possibly within the same mineralization event. Both ore minerals predated regional Neoproterozoic metamorphism. Both orebodies and host rocks have undergone extensive alteration of albite, scapolite, amphibole, biotite, sericite and chlorite. Silica and carbonate alterations are also widespread. Ore-hosting strata have a LA-ICP-MS zircon U–Pb age of 1681 ± 13 Ma, and a dolerite dyke cutting the Fe-oxide orebodies has an age of 1659 ± 16 Ma. Thus, the mineralization age of the Dahongshan deposit is constrained at between the two. All ores from the two groups have high Fe and low Ti, with variable Cu contents. Locally they are rich in Mo, Co, V, and REE, but all are poor in Pb and Zn. Sulfides from the Fe–Cu deposits have δ³⁴S values mostly in the range of +2 to +6 per mil, suggesting a mix of several sources due to large-scale leaching of the strata with the involvement of evaporites. Isotopic dating and field relationships suggest that these deposits formed in the late Paleoproterozoic. Ore textures, mineralogy and alteration characteristics are typical of IOCG-type deposits and thus define a major IOCG metallogenic province with significant implications for future exploration.     

西天山智博铁矿床磁铁矿成分特征及其矿床成因意义

智博大型磁铁矿床位于新疆西天山阿吾拉勒成矿带东段,赋存于石炭系大哈拉军山组玄武质安山岩、安山岩及火山碎屑岩中。智博铁矿床包括东、中、西以及13号矿体4个矿段。矿体主要呈层状、似层状、透镜状。金属矿物以磁铁矿为主,含少量浸染状黄铁矿,局部可见细脉赤铁矿及零星状黄铜矿。矿石构造以块状和浸染状构造为主,角砾状次之,局部为条带状构造、脉状-网脉状构造;矿石结构包括半自形-他形粒状结构、交代残余结构、板条状结构。智博矿区的蚀变矿物组合以透辉石、钠长石、钾长石、绿帘石、阳起石为主,含有少量方解石、石英、绿泥石及榍石。根据矿物共生组合、矿石结构的观察以及矿物化学分析,识别出岩浆期和热液期2个成矿期,进一步细分为3个成矿阶段:磁铁矿-透辉石-绿帘石阶段(a1),磁铁矿-钾长石-绿帘石阶段(b1),石英-硫化物阶段(b2)。磁铁矿的电子探针成分分析显示,岩浆期矿石中FeOT含量较高,而Al2O3、CaO、MgO、SiO2等氧化物含量较低,热液期矿石则相反。角砾状和部分浸染状磁铁矿中V2O5含量相对较高,与火山岩中含量类似,暗示该矿化阶段的铁质部分来源于围岩;块状以及浸染状磁铁矿FeOT含量大部分在90%以上;角砾状、网脉状、树枝状矿石中磁铁矿的w(FeOT)分布相对比较集中,多数在90%~92%之间;纹层状矿石的w(FeOT)则变化于88%~92%之间,其CaO、SiO2等氧化物平均含量相对增加。TiO2-Al2O3-MgO图解和Ca+Al+Mn vs Ti+V图解均表明智博铁矿床的形成与火山活动和岩浆热液的交代作用有关。