Applied Mineralogical Studies on Iranian Titanium Deposits

Qara-aghaj and Skandian as hard rock titanium deposit and Kahnooj one as a placer deposit were investigated from applied mineralogical point of view. The mineralogical studies were carried out using XRD, XRF, optical microscopy, scanning electron microscopy and microprobe analysis. These studies indicated that ilmenite and magnetite are main valuable minerals in the studied ores. Pyroxene, olivine and plagioclase are the main gangue minerals in Qara-aghaj ore while chlorite and plagioclase are the major gangue minerals in Skandian ore. Plagioclase, clinopyroxene, amphibole, feldspate and some quartz are the important gangue minerals in kahnooj deposit. In all three ores ilmenite is mainly in the form of ilmenite grains but some lamellae of ilmenite with thickness between 0.1 to 20 μm have been occurred as exsolution textures inside magnetite grains, where the magnetite here can be referred to as ilmenomagnetite. In the hard rock ores some fine ilmenites have been disseminated in silicate minerals. The liberation degree of granular ilmenite was determined 150, 140 and 200 μm for Qara-aghaj, Skandian and Kahnooj, respectively. So, only the granular form of ilmenite is recoverable by physical methods. Some sphene and rutile as titanium containing minerals were observed mainly inside ilmenite phase in kahnooj ore. Some fine rutile was also found inside Skandian ilmenite while there were not any other titanium minerals inside Qara-aghaj ilmenite. Apatite is another valuable mineral which was found only in Qara-aghaj ore. Using SEM and microprobe analysis it was found that there are different amounts of exsolved fine lamellae of hematite inside ilmenite in Qara-aghaj and Kahnooj ores while it was not observed in Sckandian one. The average contents of TiO2 in the lattice of Qara-aghaj, Skandian and Kahnooj ilmenite were determined 51.13, 50.9% and 52.02%, respectively. FeO content of ilmenite lattice for all three samples is clearly lower than the theoretical content. This is due to the substitution of Mg and Mn for some Fe2+ ions in the ilmenite lattice. V2O3 content of magnetite lattice is up to 1%. So, magnetite can be a suitable source for production of vanadium as a by-product in all three deposits.     

Spinels,Fe–Ti oxide minerals,apatites, and carbonates hosted in the ophiolites of Eastern Desert of Egypt: mineralogy and chemical aspects

Spinels, Fe–Ti oxide minerals, apatites, and carbonates hosted in ophiolitic serpentinites and metagabbros of Gabal Garf (southern ED) and Wadi Hammariya (central ED) of Egypt are discussed. Microscopic and electron probe studies on these minerals are made to evaluate their textural and compositional variations. Alteration of chromites led to form ferritchromite and magnetite; rutile–magnetite intergrowths and martite are common in serpentinites. Fine trillis exsolution of ilmenite–magnetite and ilmenite–hematite and intergrowth of rutile–magnetite and ilmenite–sphene are recorded. Composite intergrowth grains of titanomagnetite–ilmenite trellis lamellae are common in metagabbros. The formation of ilmenite trellis and lamellae in magnetite and titanomagnetite indicate an oxidation process due to excess of oxygen contained in titanomagnetite; trapped and external oxidizing agents. This indicates the high P _H2O and oxygen fugacity of the parental magma. The sulfides minerals include pyrrhotite, pyrite and chalcopyrite. Based on the chemical characteristics, the Fe–Ti oxide from the ophiolitic metagabbros in both areas corresponds to ilmenite. The patites from the metagabbros are identified as fluor-apatite. Carbonates are represented by dolomites in serpentinites and calcite in metagabbros. Spinel crystals in serpentinites are homogenous or zoned with unaltered cores of Al-spinel to ferritchromit and Cr-magnetite toward the altered rims. Compared to cores, the metamorphic rims are enriched in Cr# (0.87–1.00 vs. 0.83–0.86 for rims and cores, respectively) and impoverished in Mg# (0.26–0.48 vs. 0.56–0.67) due to Mg–Fe and Al (Cr)–Fe³⁺ exchange with the surrounding silicates during regional metamorphism rather than serpentinization process. The Fe–Ti oxides have been formed under temperature of ~800 °C for ilmenite. Al-spinels equilibrated below 500–550 °C, while the altered spinel rims correspond to metamorphism around 500–600 °C. Geochemical evidence of the podiform Al-spinels suggest a greenschist up to lower amphibolite facies metamorphism (at 500–600 °C), which is isofacial with the host rocks. Al-spinel cores do not appear to have re-equilibrated completely with the metamorphic spinel rims and surrounding silicates, suggesting relic magmatic composition unaffected by metamorphism. The composition of Al-spinel grains suggest an ophiolitic origin and derivation by crystallization of boninitic magma that belonging to a supra-subduction setting could form either in forearcs during an incipient stage of subduction initiation or in back-arc basins.     

Implication of Apatite and Anhydrite for Formation of an Iron‐Oxide‐Apatite (IOA) Rare Earth Element Prospect,Benjamin River,Canada

The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab₉₈Or₂–Ab₁₀₀) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An_25.3–An₆₀ in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO₄^2? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe²⁺ and release of S^2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe³⁺ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S^2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization).     

Multiphase inclusions in plagioclase from anorthosites in the Stillwater Complex,Montana: implications for the origin of the anorthosites

Multiphase inclusions, consisting of clinopyroxene+ilmenite+apatite, occur within cumulus plagioclase grains from anorthosites in the Stillwater Complex, Montana, and in other rocks from the Middle Banded series of the intrusion. The textures and constant modal mineralogy of the inclusions indicate that they were incorporated in the plagioclase as liquid droplets that later crystallized rather than as solid aggregates. Their unusual assemblage, including a distinctive manganiferous ilmenite and the presence of baddeleyite (ZrO₂), indicates formation from an unusual liquid. A process involving silicater liquid immiscibility is proposed, whereby small globules of a liquid enriched in Mg, Fe, Ca, Ti, P, REE, Zr and Mn exsolved from the main liquid that gave rise to the anorthosites, became trapped in the plagioclase, and later crystallized to form the inclusions. The immiscibility could have occurred locally within compositional boundaries around crystallizing plagioclase grains or it could have occurred pervasively throughout the liquid. It is proposed that the two immiscible liquids were analogous, n terms of their melt structures, to immiscible liquid pairs reported in the literature both in experiments and in natural basalts. For the previously reported pairs, immiscibility is between a highly polymerized liquid, typically granitic in composition, and a depolymerized liquid, typically ferrobasaltic in composition. In the case of the anorthosites, the depolymerized liquid is represented by the inclusions, and the other liquid was a highly polymerized aluminosilicate melt with a high normative plagioclase content from which the bulk of the anorthosites crystallized. Crystallization of the anorthosites from this highly polymerized liquid accounts for various distinctive textural and chemical features of the anorthosites compared to other rocks in the Stillwater Complex. A lack of correlation between P contents and chondrite-normalized rare earth element (REE) ratios of plagioclase separates indicates that the amount of apatite in the inclusions is too low to affect the REE signature of the plagioclase separates. Nevertheless, workers should use caution when attempting REE modelling studies of cumulates having low REE contents, because apatite-bearing inclusions can potentially cause problems.     

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.     

Postcumulus modification of magnetite grains in the upper zone of the Bushveld Complex,South Africa

A detailed electron microprobe study has been made of magnetite grains from magnetitite layer 1 of the upper zone of the Bushveld Complex, in order to establish if there is any evidence for postcumulus processes having affected magnetite compositions. Representative composition profiles obtained from detailed step traverses are presented for touching magnetite grains and where magnetite is in contact with either ilmenite or plagioclase.Magnetite grains in all textural settings are compositionally heterogeneous. Touching magnetite grains display systematic compositional zonations: the rims of grains show a marked decrease in Al and Mg towards the grain boundary; the cores are characterised by a distinctive peak and trough pattern for these elements. These variations can be related to the positions of exsolved phases. Exsolutions in the cores are either pleonaste or an Fe³⁺ bearing AlMg spinel, whereas those at the grain boundaries are generally more Al-rich and include corundum. Similar exsolution related compositional variations for Mg and Al were found in magnetites in contact with ilmenite and plagioclase.A model has been developed which illustrates the possible sequence of postcumulus events during the interval between accumulation of the magnetite and the cessation of subsolidus reactions. The essential feature of the model is the delicate interplay between depletion of the host magnetite by corundum, pleonaste and the Fe³⁺ bearing AlMg spinel exsolutions, and diffusion of Al and Mg into the depleted areas from the surrounding magnetite.Data for Cr contents in magnetites show that although this particular trace element is apparently resistant to redistribution by exsolution processes, it is affected by subsolidus re-equilibration between magnetite and ilmenite, or magnetite and intercumulus liquid.     

Petrological and Geochemical Constraints on the Protoliths of Serpentine‐Magnetite Ores in the Zhaoanzhuang Iron Deposit,Southern North China Craton

The uncommon Mg-rich and Ti-poor Zhaoanzhuang serpentine-magnetite ores within Taihua Group of the North China Craton(NCC) remain unclear whether the protolith was sourced from ultramafic rocks or chemical sedimentary sequences. Here we present integrated petrographic and geochemical studies to characterize the protoliths and to gain insights on the ore-forming processes. Iron ores mainly contain low-Ti magnetite(TiO_2 ~0.1 wt%) and serpentine(Mg#=92.42–96.55), as well as residual olivine(Fo=89–90), orthopyroxene(En=89–90) and hornblende. Magnetite in the iron ores shows lower Al, Sc, Ti, Cr, Zn relative to that from ultramafic Fe-Ti-V iron ores, but similar to that from metamorphic chemical sedimentary iron deposit. In addition, interstitial minerals of dolomite, calcite, apatite and anhydrite are intergrown with magnetite and serpentine, revealing they were metamorphic, but not magmatic or late hydrothermal minerals. Wall rocks principally contain magnesian silicates of olivine(Fo=83–87), orthopyroxene(En=82–86), humite(Mg#=82–84) and hornblende [XMg=0.87–0.96]. Dolomite, apatite and anhydrite together with minor magnetite, thorianite(Th-rich oxide) and monazite(LREE-rich phosphate) are often seen as relicts or inclusions within magnesian silicates in the wall rocks, revealing that they were primary or earlier metamorphic minerals than magnesian silicates. And olivine exists as subhedral interstitial texture between hornblende, which shows later formation of olivine than hornblende and does not conform with sequence of magmatic crystallization. All these mineralogical features thus bias towards their metamorphic, rather than magmatic origin. The dominant chemical components of the iron ores are SiO_2(4.77–25.23 wt%), Fe_2O_3 T(32.9–80.39 wt%) and MgO(5.72–27.17 wt%) and uniformly, those of the wall rocks are also SiO_2(16.34–48.72 wt%), Mg O(16.71–33.97 wt%) and Fe_2O_3 T(6.98–30.92 wt%). The striking high Fe-Mg-Si contents reveal that protolith of the Zhaoanzhuang iron deposit was more likely to be chemical sedimentary rocks. The distinct high-Mg feature and presence of abundant anhydrite possibly indicate it primarily precipitated in a confined seawater basin under an evaporitic environment. Besides, higher contents of Al, Ti, P, Th, U, Pb, REE relative to other Precambrian iron-rich chemical precipitates(BIF) suggest some clastic terrestrial materials were probably input. As a result, we think the Zhaoanzhuang iron deposit had experienced the initial Fe-Mg-Si marine precipitation, followed by further Mg enrichment through marine evaporated process, subsequent high-grade metamorphism and late-stage hydrothermal fluid modification.     

Genesis of a low-grade apatite-ilmenite-magnetite deposit in the Kauhajärvi gabbro, western Finland

The Paleoproterozoic Kauhajärvi gabbro is one of several Fe-, Ti-, and P-rich mafic intrusions associated with granitoids in the Fennoscandian shield in western Finland. The gabbro is cut by the late-orogenic Lauhanvuori granite (ca.1870?Ma), whereas the surrounding area is composed of synorogenic, collision-related granitoids and calc-alkaline volcanic rocks (ca. 1890?Ma) belonging to the Mid Finland Granitoid Complex. The mafic intrusions were probably emplaced into a Svecofennian rift zone. They are characterized by a high phosphorus content; the common occurrence of ilmenite as separate grains; and the coeval crystallization of apatite, Fe-Ti oxides, and Fe-Mg silicates. The Kauhajärvi gabbro is composed of two geochemically and structurally distinct zones. The basal zone is composed of poorly-layered, fine- to medium-grained gabbro, which represents an early intrusion of tholeiitic magma, and has rather high concentrations of chromium, magnesium and silica. Typically, the concentrations of iron, titanium and phosphorus are low, except for the top that is enriched in apatite and ilmenite. During most of the crystal-liquid fractionation of the basal zone magma, low f _O2 limited the crystallization of Fe-Ti-oxides. Instead, titanium became enriched in the uppermost layer of the basal zone. The main zone represents a later injection of more evolved tholeiitic magma and makes up 80 to 90%of the total intrusion volume. Peridotite is common, along with gabbro and gabbronorite, in the lower and middle parts of the main zone, and anorthosite is common near the top of the main zone. The Mg:Fe ratio in mafic minerals and vanadium concentrations in magnetite decrease upwards. The variation within the main zone can be explained by crystal-liquid fractionation of a single batch of a parental magma under conditions of relatively high f _O2. Titanium is not progressively enriched. The ratio of titanium to iron (TiO₂/Fe₂O₃ = 0.16 to 0.20; Fe total as Fe₂O₃) is constant in the main zone and normal for mafic intrusions. Titanium is sited in separate ilmenite grains and in lamella within ilmenomagnetite (Ti-bearing magnetite). The high phosphorus content in the main zone is interpreted to result in crystallization of ilmenite and ilmenomagnetite instead of Ti-rich magnetite under relatively high f _O2 conditions. High concentrations of titanium, iron and phosphorus in rocks of the main zone can be explained by pre-emplacement crystal-melt fractionation in a deep magma reservoir and/or contamination of mantle-derived mafic magmas by granitic magmas from partial melting of crustal rocks. A low-grade Fe-Ti-P resource at Kauhajärvi consists of layers with as much as 20 wt. % combined ilmenite (usually 8 to 11 wt. %), apatite (1 to 8 wt. %) and magnetite (1 to 9 wt. %). Mineralized layers are of variable thickness (2?m to 30?m) and occur in variable host rocks (peridotite or gabbro). The Fe-Ti oxides are most abundant in peridotite and pyroxene- or olivine-rich gabbronorite within the main zone. The contact between mineralized rocks (4%TiO₂) and non- or slightly-mineralized rocks is gradual. The deposit as a whole consists of three to five mineralized layers with maximum combined thickness of 70?m. Apatite is most abundant in the oxide-rich layers, but is locally also concentrated in anorthosite with low Fe-Ti oxide contents. The weight ratio of ilmenite to magnetite is 3:2. The ratio of total Ti-Fe-oxides to apatite averages 4.0, with the range of 1.5 to >15.     

In-situ LA-ICP-MS trace elemental analyses of magnetite: Fe–Ti–(V) oxide-bearing mafic–ultramafic layered intrusions of the Emeishan Large Igneous Province,SW China

The Taihe, Baima, Hongge, Panzhihua and Anyi intrusions of the Emeishan Large Igneous Province (ELIP), SW China, contain large magmatic Fe–Ti–(V) oxide ore deposits. Magnetites from these intrusions have extensive trellis or sandwich exsolution lamellae of ilmenite and spinel. Regular electron microprobe analyses are insufficient to obtain the primary compositions of such magnetites. Instead, laser ablation ICP-MS uses large spot sizes (~ 40 μm) and can produce reliable data for magnetites with exsolution lamellae. Although magnetites from these deposits have variable trace element contents, they have similar multi-element variation patterns. Primary controls of trace element variations of magnetite in these deposits include crystallography in terms of the affinity of the ionic radius and the overall charge balance, oxygen fugacity, magma composition and coexisting minerals. Early deposition of chromite or Cr-magnetite can greatly deplete magmas in Cr and thus Cr-poor magnetite crystallized from such magmas. Co-crystallizing minerals, olivine, pyroxenes, plagioclase and apatite, have little influence on trace element contents of magnetite because elements compatible in magnetite are incompatible in these silicate and phosphate minerals. Low contents and bi-modal distribution of the highly compatible trace elements such as V and Cr in magnetite from Fe–Ti oxide ores of the ELIP suggest that magnetite may not form from fractional crystallization, but from relatively homogeneous Fe-rich melts. QUILF equilibrium modeling further indicates that the parental magmas of the Panzhihua and Baima intrusions had high oxygen fugacities and thus crystallized massive and/or net-textured Fe–Ti oxide ores at the bottom of the intrusive bodies. Magnetite of the Taihe, Hongge and Anyi intrusions, on the other hand, crystallized under relatively low oxygen fugacities and, therefore, formed net-textured and/or disseminated Fe–Ti oxides after a lengthy period of silicate fractionation. Plots of Ge vs. Ga + Co can be used as a discrimination diagram to differentiate magnetite of Fe–Ti–(V) oxide-bearing layered intrusions in the ELIP from that of massif anorthosites and magmatic Cu–Ni sulfide deposits. Variable amounts of trace elements of magmatic magnetites from Fe–Ti–(P) oxide ores of the Damiao anorthosite massif (North China) and from Cu–Ni sulfide deposits of Sudbury (Canada) and Huangshandong (northwest China) demonstrate the primary control of magma compositions on major and trace element contents of magnetite.     

Microtextures of opaque inclusions: their use as indicators for hiatuses during garnet porphyroblast growth

Within an analysed garnet porphyroblast, opaque inclusions imaged with the backscatter facility of a scanning electron microscope show different microtextures depending on their position within the porphyroblast. Three different zones can been distinguished: Zone 1 contains a Ti‐rich magnetite that has decomposed to a symplectite of fine and narrowly spaced exsolution lamellae of ilmenite and magnetite. Zone 2 shows a Ti‐rich magnetite symplectite with thicker and more widely spaced exsolution lamellae of ilmenite and magnetite. Within zone 3, Ti‐rich magnetite symplectite has totally been replaced by recrystallized magnetite crystals bordered by a thin ilmenite rim. Similar microtextures within ulvöspinel‐rich magnetite have elsewhere shown to be the result of an increase in oxidation and rate of diffusion. During metamorphism of metapelites, such an increase can be reasonably envisaged because of dehydration reactions progressing during rising temperatures, and this has occurred during the overgrowth of the three different microtextures by the garnet porphyroblast. Because the microtextures are homogeneous within the three different zones, it is deduced that the oxidation reaction rate of the opaque inclusions was substantially lower than the garnet growth rate. As a consequence, hiatuses in the garnet growth history must have occurred between the evolution from one microtexture to the next. A comparison between the inclusion trail geometry and the microtextural zone boundaries shows a perfect coincidence between these and the sites where inclusion trails become strongly deflected and truncated. This correlation confirms that, in the studied case, sharp microstructural boundaries (as truncation zones or deflection zones) coincide with growth hiatuses. The study therefore highlights the potential use of opaque inclusions to confirm or reject the occurrence of growth hiatuses within garnet porphyroblasts, especially in cases where discontinuities in the inclusion trail patterns are otherwise arbitrarily associated with growth hiatuses.     

Composition and Assemblage Characteristics of Magnetic Minerals in Layer S_(5-1) of Xifeng and Duanjiapo Sections

Magneticmineralsintheloess paleosolseriesaccountforabout 1 % -2 %ofthetotal (LiuTungshengandZhangZhonghu ,1 962 ) .Duetotheiraerolianorigin ,themagneticmineralsarecomplicatedincomposition ,largeingrainsizerange ,andsignificantlydifferentincrystallinity .Asaresult,researchonthesemagneticmineralswouldbesetwithalotofdifficulties.Previousre searchersemployedopticalmicroscopic ,X raydiffractionandM ssbauerspectrometrictechniquestostudythemagneticmineralsintheloess paleosolseries,andchieflyontheb…     

Magnetite Dyke in Precambrian Banded Iron Formation,Singhbhum Craton,India: Mineralogical and Chemical Characteristics

Banded iron formation (BIF) of the Gorumahisani–Sulaipat–Badampahar (GSB) belt in Singhbhum Craton, India, consists predominantly of magnetite. This BIF is intruded by a magnetite dyke. The magnetite dyke is massive and compact with minor sulphide minerals while the host banded magnetite ore, a component of the BIF, shows thin lamination. The magnetite ore of the dyke is fine to medium grained and exhibits interlocking texture with sharp grain boundaries, which is different from the banded magnetite that is medium to coarse grained and show irregular martitised and goethitised grain boundaries. Relics of Fe–Ca–Mn–Mg‐carbonate and iron silicates (grunerite and cummingtonite) are observed in the banded magnetite. The intrusive magnetite is distinctly different in minor, trace and REE geochemistry from the banded magnetite. The banded magnetite contains higher amounts of Si, Al, Mn, Ca, Mg, Sc, Ga, Nb, Zr, Hf, Co, Rb and Cu. In contrast, the massive magnetite is enriched in Cr, Zn, V, Ni, Sr, Pb, Y, Ta, Cs and U with higher abundance of HREE. In the chondrite normalized plot, the massive magnetite shows a slight positive Eu anomaly while the banded ore does not show any Eu anomaly. Field disposition, morphology, mineralogy and chemistry show that the intrusive magnetite dyke is of igneous origin, while magnetite in BIF formed from a carbonate protolith through the process of sedimentation.     

Hydrothermal H?gbomite Associated with Vanadiferous-Titaniferous (V-Ti) Bearing Magnetite Bands in Bhakatarhalli Chromite Mine, Nuggihalli Greenstone Belt, Western Dharwar Craton, Karnataka, India

Hogbomite,a rare exotic mineral,is found to be associated with the vanadiferous-titaniferous （V-Ti） bearing magnetite bands at Bhakatarhalli,Nuggihaifi greenstone belt,western Dharwar Craton,India.We report on a second occurrence of hogbomite from the Dharwar craton in Karnataka,which is the sixth documented occurrence of this mineral from India.We evaluate the chemical characteristics of hogbomite and associated Fe-Ti-minerals in an attempt to identify its formation as a primary hydrothermal mineral in a metamorphosed magnetite layer.We report here the presence of hogbomite as a complex oxide of Fe,Mg,Al and Ti with accessory of Zn,V and Sn.Petrographic studies suggest the （V-Ti） bearing magnetite （Mt） contain spinel,hogbomite,chlorite,martite,ilmenite （Ⅱ） and minor amounts of diaspore.The hogbomite displays euhedral to subhedral textures,and is up to 250 μm along the grain boundaries of magnetite and ilmenite.In the samples studied,hogbomite is prismatic,irregular and elongated in shape.The genesis of hogbomite in veins between magnetite and ilmenite implies its precipitation from fluids without involving complicated reactions.Several models were proposed for the formation of hogbomite; however,the subject is still debatable.     

Hydrothermal alteration, fluid flow and volume change in shear zones: the layered mafic–ultramafic Kettara intrusion (Jebilet Massif, Variscan belt, Morocco)

During emplacement and cooling, the layered mafic–ultramafic Kettara intrusion (Jebilet, Morocco) underwent coeval effects of deformation and pervasive fluid infiltration at the scale of the intrusion. In the zones not affected by deformation, primary minerals (olivine, plagioclase, clinopyroxene) were partially or totally altered into Ca‐amphibole, Mg‐chlorite and CaAl‐silicates. In the zones of active deformation (centimetre‐scale shear zones), focused fluid flow transformed the metacumulates (peridotites and leucogabbros) into ultramylonites where insoluble primary minerals (ilmenite, spinel and apatite) persist in a Ca‐amphibole‐rich matrix. Mass‐balance calculations indicate that shearing was accompanied by up to 200% volume gain; the ultramylonites being enriched in Si, Ca, Mg, and Fe, and depleted in Na and K. The gains in Ca and Mg and losses in Na and K are consistent with fluid flow in the direction of increasing temperature. When the intrusion had cooled to temperatures prevailing in the country rock (lower greenschist facies), deformation was still active along the shear zones. Intense intragranular fracturing in the shear zone walls and subsequent fluid infiltration allowed shear zones to thicken to metre‐scale shear zones with time. The inner parts of the shear zones were transformed into chlorite‐rich ultramylonites. In the shear zone walls, muscovite crystallized at the expense of Ca–Al silicates, while calcite and quartz were deposited in ‘en echelon’ veins. Mass‐balance calculations indicate that formation of the chlorite‐rich shear zones was accompanied by up to 60% volume loss near the centre of the shear zones; the ultramylonites being enriched in Fe and depleted in Si, Ca, Mg, Na and K while the shear zones walls are enriched in K and depleted in Ca and Si. The alteration observed in, and adjacent to the chlorite shear zones is consistent with an upward migrating regional fluid which flows laterally into the shear zone walls. Isotopic (Sr, O) signatures inferred for the fluid indicate it was deeply equilibrated with host lithologies.     

Trace Element Geochemistry of Magnetite from the Fe(-Cu) Deposits in the Hami Region, Eastern Tianshan Orogenic Belt, NW China

Laser ablation–inductively coupled plasma–mass spectrometry(LA–ICP–MS) was used to determine the trace element concentrations of magnetite from the Heifengshan, Shuangfengshan, and Shaquanzi Fe(–Cu) deposits in the Eastern Tianshan Orogenic Belt. The magnetite from these deposits typically contains detectable Mg, Al, Ti, V, Cr, Mn, Co, Ni, Zn and Ga. The trace element contents in magnetite generally vary less than one order of magnitude. The subtle variations of trace element concentrations within a magnetite grain and between the magnetite grains in the same sample probably indicate local inhomogeneity of ore–forming fluids. The variations of Co in magnetite between samples are probably due to the mineral proportion of magnetite and pyrite. Factor analysis has discriminated three types of magnetite: Ni–Mn–V–Ti(Factor 1), Mg–Al–Zn(Factor 2), and Ga– Co(Factor 3) magnetite. Magnetite from the Heifengshan and Shuangfengshan Fe deposits has similar normalized trace element spider patterns and cannot be discriminated according to these factors. However, magnetite from the Shaquanzi Fe–Cu deposit has affinity to Factor 2 with lower Mg and Al but higher Zn concentrations, indicating that the ore–forming fluids responsible for the Fe–Cu deposit are different from those for Fe deposits. Chemical composition of magnetite indicates that magnetite from these Fe(–Cu) deposits was formed by hydrothermal processes rather than magmatic differentiation. The formation of these Fe(–Cu) deposits may be related to felsic magmatism.     

The origin of rutile-ilmenite aggregates (“nigrine”) in alluvial-fluvial placers of the Hagendorf pegmatite province, NE Bavaria, Germany

Summary Titanium placer deposits occur in alluvial-fluvial drainage systems which dissect Moldanubian gneisses intruded by Late Variscan pegmatites (Hagendorf province) in southern Germany. Based upon their texture (zonation, exsolution lamellae, intergrowth), microchemical data (Nb, Cr, Ta, V, Fe, W, Sn) and mineral inclusions, two major grain types of intergrown rutile and ilmenite have been established. Grains of type A are always zoned and consist of rutile cores enveloped by ilmenite containing small inclusions of wolframite. A core-rim transition zone is characterized by complex relations of rutile and ilmenite, with rutile lamellae being rich in Nb, V and Fe. Types B1 and B2 aggregates consist of ilmenite with lamellae of niobian rutile and/or ilmenorutile, and additionally have inclusions of ferrocolumbite, pyrochlore, betafite, sphalerite, pyrrhotite and Fe oxides. Such grain types featuring an intimate intergrowth of rutile and ilmenite were called nigrine. Type-C grains are quite similar in their morphological appearance but consist of W-enriched rutile devoid of mineral inclusions and reaction products. Pseudorutile and leucoxene replacing minerals of the nigrine aggregates are presumably caused by supergene alteration under fluctuating redox conditions. Phosphate and aluminum remobilized by supergene processes led to the formation of hydrous Ti-rich phases containing Al, P and Fe. High Nb and W concentrations in nigrine aggregates and in rutile type C may be taken as a marker for highly differentiated granites or pegmatites. This has implications for both, heavy-mineral-based provenance analysis and stream sediment exploration.     

Mechanisms of retrograde changes in oxide minerals from the Proterozoic Serrote da Laje deposit,northeastern Brazil

Retrograde textural and chemical changes in oxide minerals from the Proterozoic Serrote da Laje deposit, northeastern Brazil, have been investigated. The deposit is situated in a mafic-ultramafic layered sill. Oxidation and cooling leading to successively decreasing diffusion rates resulted in disequilibrium on the microscale. Pleonaste in particular shows a rapid change in composition between (a) coarse grains in a granoblastic magnetite host, indicating metamorphic peak conditions, (b) coarse lamellae in magnetite, indicating commencement of exsolution, and (c) composite pleonaste — ilmenite lamellae in magnetite, which indicate oxidation exsolution. Barren rock layers cooled under more oxidized conditions compared with oxide-rich layers. Formation of pleonaste- and ilmenite lamellae in magnetite and ilmenite — hematite relations are discussed.     

Textural re-equilibration,hydrothermal alteration and element redistribution in Fe-Ti oxide pods,Singhbhum Shear Zone,eastern India

This study describes textures and mineral chemistry of magnetite-ilmenite-bearing pods/pockets in mineralogically diverse feldspathic schist near Pathargora in the Singhbhum Shear Zone, eastern India. The textural and geochemical characteristics of the magnetite-ilmenite assemblage are the results of a protracted geological history involving magmatic crystallization and oxidation-exsolution of titanomagnetite, deformation-induced recrystallization and textural re-equilibration and hydrothermal fluid-induced hematitization of magmatic magnetite. The magnetite grains contain characteristic trellis and sandwich ilmenite lamella, which are interpreted to be the products of oxidation-exsolution of ulvöspinel component of magnetite-ulvöspinel solid solution. The exsolution process was accompanied by preferential partitioning of spinel elements such as Cr, Al and V in magnetite and Ti, Mn, Mg, HFS elements (Nb, Ta), transition elements (Sc, Co, Cu and Zn) and granitophile elements (Mo, Sn and W) in ilmenite. The deformed sandwich lamella is locally recrystallized and transformed into granular ilmenite close to fractures, micro-shear planes and magnetite grain boundaries. Coarse granules of ilmenite, within or associated with magnetite, are of two textural types: one invariably contains Fe-rich exsolved phase and may be of magmatic origin, while the other mostly formed by strain-induced, fluid-mediated expulsion (from the interior of magnetite to its boundary) and dynamic recrystallization of existing ilmenite lamella in magnetite, and dynamic recrystallization of primary ilmenite containing Fe-rich exsolved phases. Magnetite is variably hematitized. The highly porous nature and trace element geochemistry of hematite and mass-balance calculations suggest the hematitization was mostly redox-independent and was caused by infiltration of metal-rich, reduced and acidic fluid. The hematitization process was associated with significant enrichment and immobilization of U, Th, Pb, REEs, Cu, Mo and W and depletion of Ni, Cr, V in hematite.     

The normative mineralogy of 10 soil profiles in Fennoscandia and north-western Russia

The mineralogical composition of soil horizons in different soil types of different ages was estimated by applying the NORMA software, which was developed originally for calculating the normative mineralogical composition of young podsols. Ten soil profiles from six sites in NW Russia, two in Finland, and one in NE Norway were sampled in 1999 as a part of the pilot phase of a large geochemical mapping project. Total element concentrations were determined from the <2 mm fraction by XRF from powdered pellets for Al, Ca, Cr, Fe, K, Mg, Mn, Na, P, S, Si, Ti, and Zr, and for Ba by ICP-AES after HF+HClO₄ extraction. Extractable concentrations for Al, Ca, Cr, Fe, K, Mn, Mg, Na, P, S, Ti, Zr, and Ba were determined by ICP-MS or ICP-AES after aqua regia (a 1:3 mixture of strong HCl and HNO₃) extraction. Total C was determined using a thermal conductivity detector from a sample burned in an O₂ stream. The NORMA software was used to calculate the percentage of normative soluble minerals pyrite, apatite, titanite, calcite, biotite, chlorite, weathered albite, hydrous Al-silicate, goethite and soluble residue. The percentages of non-soluble normative minerals rutile, hornblende, K-feldspar, albite, anorthite, tremolite, wollastonite, kaolinite, magnetite, zircon, quartz, carbon (graphite), and non-soluble residue were calculated after soluble minerals.The calculated mineralogical composition of C-horizon samples in each profile reflected the known geological composition of the bedrock from which the soil parent material was derived during geological processes. Secondary minerals including goethite and hydrous Al-silicates, were detected in upper soil horizons reflecting the development of soils. Rather than age, the local bedrock geology together with the mineralogical composition and chemical properties of the parent material proved to be the controlling factor in the formation of secondary minerals. The results showed that the NORMA method can be used in defining the mineralogy of soil horizons in a large variety of soil types.     

Composition and assemblage characteristics of magnetic minerals in layer S<Subscript>5-1</Subscript> of Xifeng and Duanjiapo sections

Relatively strongly magnetic fine components (< 30μm, XS-4J and DS-4J) which are most environmentally sensitive were separated from layer S_5-1 in the Xifeng and Duanjiapo loess sections and analyzed by MPV-3 for their morphometric characteristics and reflectance, SEM-ESD for their element contents and XRD for their mineral phases, respectively. The results showed that minerals in both samples are dominated by detrial Fe-Ti oxides of aeolian origin. In sample XS-4J the reflectance and iron contents of magnetic minerals are usually high. In addition to magnetite (Fe₃O₄), maghemite (γFe₂O₃) and hematite (Fe₂O₃), some Fe-high oxide (72.25 wt%–86.67 wt%), ilmenite (FeTiO₃), and magnetite-ulvöspinel [Fe(FeCr)O₄, Fe (FeNi)O₄] were also detected. In sample DS-4J obvious negative linear correlations were found between Ti and Fe, and the contents of Mn, Si, Al and Ca are usually high and the minerals are dominated by magnetite (maghemite), goethite (FeOOH) and limonite (containing Si and OH). In addition, the signs of corrosion of magnetic minerals and newly crystallized magnetite (maghemite) were recognized. Differences in the composition and assemblage characteristics of magnetite minerals between XS and DS reflect significant differences in source rocks and preserving conditions.