Isoferroplatinum mineral assemblage in the northwestern Salair gold placer

Isoferroplatinum mineral assemblage has been first discovered in the Simonovsky Brook gold placer localized in the Egor'evskoe gold-bearing district (Salair Range). It includes isoferroplatinum (Pt₃Fe) grains with inclusions of cuprorhodsite CuRh₂S₄, braggite (Pt,Pd)S, vysotskite PdS, high-Pt rhodarsenide (Rh,Pd,Pt)₂As, keithconnite Pd₃Te, hollingworthite RhAsS, Cu and Fe sulfides, basic plagioclase, magnetite, epidote, quartz, kaolinite, and leucoxene. The assemblage might have been produced from small gabbroid bodies widespread in the northwestern Salair region, including those of the Uralian platinum-bearing type, or from gabbroids of other complexes.     

Platinum-group mineral assemblage of the Prizhimny Creek (Koryak Highland)

In the alluvial deposits of the Prizhlimny Creek (southern part of the Koryak Highland), grains of platinum-group minerals are found along with gold. We have established that the grains are native platinum (Pt, Fe) containing Cu (up to 5 wt.%), Os (up to 8 wt.%), and Rh (up to 2 wt.%). Inclusions in the platinum are native osmium (the content of Ir impurity reaches 12 wt.%, the average content being 0.2–4 wt.%), an unnamed intermetallic compound of composition PtRh, sulfides and arsenides of PGE (cooperite, laurite, malanite, cuproiridsite, cuprorhodsite, sperrylite, hollingworthite, unnamed compounds PdS, (Ir,Ru)S₂, (Ir,Pt)S₂, Cu, and Fe (bornite, chalcopyrite), chromite, and Cr-magnetite. Replacement of native-osmium crystals by compound IrO₂ is described. It has been established that this compound formed during oxidation accompanied by the replacement of isoferroplatinum by native platinum. The data obtained agree with the results of study of platinum-group mineral assemblages from placers localized in weakly eroded Ural–Alaskan-type massifs whose apical parts formed under high oxygen activity conditions. Clinopyroxenites of the Prizhimny massif are considered to be the potential source of PGE.     

Gold and platinum group minerals in placers of the South Urals: Composition,microinclusions of ore minerals and primary sources

Gold and platinum group minerals from the gold placers of the South Urals are studied in order to identify the metal sources. In placers from the Main Uralian fault zone (MUF), the primary gold contains Ag (up to 29 wt.%), Cu (up to 2 wt.%) and Hg (up to 4 wt.%) and its fineness ranges from 538 to 997‰. Tetra-auricupride and cupriferous gold (up to 20 wt.% Cu) are common for the Nizhny Karabash placer of the MUF zone. In the eastern part of the South Urals, the placer gold is mainly characterized by high fineness of 900–1000‰ and low Cu contents (max 1.38 wt.%). Most of the placer gold grains consist of the primary domains, which are rimmed by secondary high-fineness gold with diffuse and clear boundaries. The secondary gold also develops along the shear dislocations of primary gold. Gold contains microinclusions of geerite, balkanite, chalcopyrite, Se-bearing galena, sphalerite, pyrite, pyrrhotite, arsenopyrite and hematite.Twenty four (including five unnamed) platinum group minerals (PGMs) were found in 28 placers; those from the Kialim and Maly Iremel placers of the Miass placer zone were studied in details. In the Kialim placer, ruthenium is most abundant PGM, which hosts microinclusions of isoferroplatinum, ferroan platinum, laurite, cupriferous gold, a mineral similar in composition to tolovkite, heazlewoodite and unnamed RhSbS phase. The osmium contains microinclusions of erlichmanite and laurite. The iridium grains hosts various sulfides and arsenides of platinum group elements (PGEs). The inclusion-free PGMs form Ru compositional trend in contrast to Os–Ru trend of the Ir-depleted inclusion-hosted PGMs. The isoferroplatinum from the Maly Iremel placer hosts laurite, rhodarsenite, bowieite, a mineral similar in composition to miassite and unnamed sulfide of Pt (Pt_1.11S_2.00) and antimonide of Pd ((Pd_2.41Rh_0.43Fe_0.17)_3.01(Sb_0.91Te_0.09)_1.00). Ruthenium is a host to isoferroplatinum, PGE sulfides and arsenides, and heazlewoodite. Osmium contains microinclusions of ferroan platinum; iridium is a host to a mineral similar in composition to hongshiite. Three types of PGM intergrowths were identified in the Maly Iremel samples: (1) the intergrowths of platy grains of ruthenium with isoferroplatinum and a mineral similar in composition to tulameenite; (2) the open-latticework intergrowths of platy crystals of ruthenium with interstitial aggregates made up of gold, isoferroplatinum and a mineral similar in composition to xingzhongite and (3) the intergrowths of osmium and irarsite and iridarsenite, which are developed along cleavage of the osmium grains. Nickel sulfides associated with some PGMs contain Ru (11.32 wt.%) and Rh (2.21 wt.%) in millerite and Ir (31.00 wt.%), Ru (5.81 wt.%) and Rh (2.87 wt.%) in vaesite.The primary metal sources were determined on the basis of the mineral assemblages and composition of minerals, taking into account the nearby mineral deposits and directions of rivers. The rodingite-associated gold, gold-bearing massive sulfide and chromite deposits are major sources of gold and PGMs in placers of the Miass placer zone confined to the MUF structure of the South Urals. In the southern part of this structure, gold was mainly originated from orogenic gold–sulfide deposits associated with volcanic/volcaniclastic rocks and listvenite-associated gold deposits. The placer PGMs were derived from the adjacent ultramafic massifs of ophiolitic origin. The distance between the placers and primary deposits varies from 2 to 5 km (up to 20 km in the extended valley of the Miass River). Usage of ore microinclusions and associated PGMs in study of placer gold is far more advanced than an ordinary consideration of gold composition alone. This approach allowed us to identify the concrete sources for individual placers and to predict some mineralogical findings in already known primary occurrences.     

Mineral inclusions in Fe-Pt solid solution from the alluvial ore occurrences of the Anabar basin (northeastern Siberian Platform)

This study is concerned with the typochemical features of heavy-concentrate platinum from diamond placers of the Mayat-Vodorazdel’nyi site in the Anabar River basin. Platinum occurs there as Fe-Pt solid solutions (ferroan platinum of Ru-Rh specialization, ~ 90%), as well as minor Pd- and Ir-ferroplatinum. Among PGE minerals, Os-Ir-Ru alloys and chengdeite are revealed. Inclusions of PGE minerals are thoroughly studied, and the scales of their spread, the composition of mineral phases, and the relations between them are determined. Ruthenium-containing high-Rh ferroplatinum bears a lot of inclusions of Rh-S composition: Rh-containing PGE thiospinels and sulfides and arsenides of Rh, Ru, and Pt. In low-Rh platinum, mineral inclusions are much scarcer and usually form other parageneses. The mineral compositions in the system Rh-S-Ru indicate to the existence of a long isomorphous series Rh₃S₄-Ru₃S₄, with the content of Ru₃S₄ reaching 15 at.%.     

PGE Mineralization of Massive Chromitites of the Iov Dunite Body (Northern Urals)

This work presents the results of the first comprehensive study of PGE mineralization from massive chromitites of the Iov dunite body (Northern Urals). The chromitites are composed of chromespinelides with a higher content of Cr₂O₃ with respect to those from other zonal clinopyroxenite–dunite massifs of the Urals. However, the composition of chromespinelides fits the trend that is characteristic of the dunite–clinopyroxenite–gabbro formation. PGE minerals, in particular Pt–Fe solid solutions, were identified in chromitites and in chromespinelides in the form of crystals and aggregates of a complex non-crystallographic habit and less often of an idiomorphic cubic habit. In terms of stoichiometry, Pt–Fe minerals correspond to ferroplatinum (Pt₂Fe) and isoferroplatinum (Pt₃Fe). The minerals of the isomorphic tetraferroplatinum–tulameenite–nickelferroplatinum series are widely distributed. Thus, the PGE mineralization of the Iov dunite body has features that are characteristic of clinopyroxenite–dunite massifs of the Urals.     

Colloform high-purity platinum from the placer deposit of Koura River (Gornaya Shoriya,Russia)

A microinclusion of colloform high-purity platinum in a grain of platinum-group minerals (PGM) from the alluvial gold-bearing placer deposit in the south of Western Siberia (Russia) was detected and characterized for the first time. It is different in composition, texture, and conditions of formation from high-purity platinum of other regions described in the literature. The main characteristics of investigated high-purity platinum are colloform-layered texture, admixture of Fe (0.37–0.78 wt%), and paragenesis of Cu-rich isoferroplatinum, hongshiite, and rhodarsenide. The PGM grain with high-purity platinum is multiphase and heterogeneous in texture. It is a product of intensive metasomatic transformation of Cu-rich isoferroplatinum (Pt₃(Fe_0.6Cu_0.4)). The transformation was carried out in two stages: 1 – copper stage including three substages (Cu-rich isoferroplatinum, copper platinum and hongshiite); and 2 – arsenic (rhodarsenide). The formation of high-purity platinum was separated in time from the formation of isoferroplatinum and was carried out by precipitation from postmagmatic solutions.     

<Superscript>190</Superscript>Pt–<Superscript>4</Superscript>He age of PGE ores in the Alkaline–Ultramafic Kondyor Massif (Khabarovsk District,Russia)

A new ¹⁹⁰Pt–⁴He method for dating isoferroplatinum has been developed at the Institute of Precambrian Geology and Geochronology, Russian Academy of Sciences. Here we publish the first results of dating of isoferroplatinum from the main mineralogical and geochemical types of PGE mineralization in dunite. The obtained ¹⁹⁰Pt–⁴He age of isoferroplatinum is 129 ± 6 Ma. The gained ¹⁹⁰Pt–⁴He age of isoferroplatinum specimens of different genesis (magmatic, fluid–metamorphogenic, and metasomatic) from the Kondyor Massif indicates that the PGM mineralization took place synchronously and successively with evolution of primarily picrite, followed by subalkaline and alkaline melts of the Mesozoic tectonic–magmatic activation of the Aldan Shield.     

Platinum-group Mineral (PGM) and Base-metal Sulphide (BMS) Inclusions in Chromitites of the Zedang Ophiolite, Southern Tibet, China and their Petrogenetic Significance

Voluminous platinum-group mineral(PGM) inclusions including erlichmanite(Os,Ru)S_2, laurite(Ru,Os)S_2, and irarsite(Ir,Os,Ru,Rh)As S, as well as native osmium Os(Ir) and inclusions of base metal sulphides(BMS), including millerite(NiS), heazlewoodite(Ni_3S_2), covellite(CuS) and digenite(Cu_3S_2), accompanied by native iron, have been identified in chromitites of the Zedang ophiolite, Tibet. The PGMs occur as both inclusions in magnesiochromite grains and as small interstitial granules between them; most are less than 10 μm in size and vary in shape from euhedral to anhedral. They occur either as single or composite(biphase or polyphase) grains composed solely of PGM, or PGM associated with silicate grains. Os-, Ir-, and Ru-rich PGMs are the common species and Pt-, Pd-, and Rh-rich varieties have not been identified. Sulfur fugacity and temperature appear to be the main factors that controlled the PGE mineralogy during crystallization of the host chromitite in the upper mantle. If the activity of chalcogenides(such as S, and As) is low, PGE clusters will remain suspended in the silicate melt until they can coalesce to form alloys. Under appropriate conditions of ?S_2 and ?O_2, PGE alloys might react with the melt to form sulfides-sulfarsenides. Thus, we suggest that the Os, Ir and Ru metallic clusters and alloys in the Zedang chromitites crystallized first under high temperature and low ?S_2, followed by crystallization of sulphides of the laurite-erlichmanite, solid-solution series as the magma cooled and ?S_2 increased. The abundance of primary BMS in the chromitites suggests that ?S_2 reached relatively high values during the final stages of magnesiochromite crystallization. The diversity of the PGE minerals, in combination with differences in the petrological characteristics of the magnesiochromites, suggest different degrees of partial melting, perhaps at different depths in the mantle. The estimated parental magma composition suggests formation in a suprasubduction zone environment, perhaps in a forearc.     

Platinum group element mineralization of the Svetly Bor and Veresovy Bor clinopyroxenite–dunite massifs,Middle Urals,Russia

The new data for the geology and mineralogy of the platinum group element (PGE) mineralization related to the chromite–platinum ore zones within the dunite of the Svetly Bor and Veresovy Bor massifs in the Middle Urals are discussed. The geological setting of the chromite–platinum ore zones, their platinum content, compositional and morphological features of the platinum group minerals (PGM) are compared to those within the Nizhny Tagil massif, the world standard of the zonal complexes in the Platinum Ural belt. The chromite–platinum orebodies are spatially related to the contacts between differently granular dunites. Majority of PGM are formed by Pt–Fe alloys that are close in terms of stoichiometry to isoferroplatinum (Pt₃Fe), and associated with Os–Ir alloys, Ru–Os and Ir–Rh sulfides, and Ir–Rh thiospinels of the cuproiridsite–cuprorhodsite–ferrorhodsite solid solution. The tetraferroplatinum (PtFe)–tulameenite (PtFe_0.5Cu_0.5) solid solution and Pt–Cu alloys belong to the later PGM assemblage. The established features of the chromite–platinum ore zones testify to the highly probable identification of the PGE mineralization within the dunite of the Svetly Bor and Vesesovy Bor massifs and could be used in prospecting and exploration for platinum.     

Origin of primary PGM assemblage in сhromitite from a mantle tectonite at Harold’s Grave (Shetland Ophiolite Complex, Scotland)

In this paper we present textural and mineral chemistry data for a PGM inclusion assemblage and whole-rock platinum-group element (PGE) concentrations of chromitite from Harold’s Grave, which occurrs in a dunite pod in a mantle tectonite at Unst in the Shetland Ophiolite Complex (SOC), Scotland. The study utilized a number of analytical techniques, including acid digestion and isotope dilution (ID) ICP-MS, hydroseparation and electron microprobe analysis. The chromitite contains a pronounced enrichment of refractory PGE (IPGE: Os, Ir and Ru) over less refractory PGE (PPGE: Rh, Pt and Pd), typical of mantle hosted ‘ophiolitic’ chromitites. A ‘primary’ magmatic PGM assemblage is represented by euhedrally shaped (up to 60 μm in size) single and composite inclusions in chromite. Polyphase PGM grains are dominated by laurite and osmian iridium, with subordinate laurite + osmian iridium + iridian osmium and rare laurite + Ir-Rh alloy + Rh-rich sulphide (possibly prassoite). The compositional variability of associated laurite and Os-rich alloys at Harold’s Grave fit the predicted compositions of experiment W-1200-0.37 of Andrews and Brenan (Can Mineral 40: 1705–1716, 2002) providing unequivocal information on conditions of their genesis, with the upper thermal stability of laurite in equilibrium with Os-rich alloys estimated at 1200–1250 °C and f(S₂) of 10^?0.39–10^?0.07.     

The mineralogy and mineral associations of platinum group elements and gold in the Platreef at Zwartfontein, Akanani Project, Northern Bushveld Complex, South Africa

The mineralogy of the platinum-group elements (PGE), and gold, in the Platreef of the Bushveld Complex, was investigated using an FEI Mineral Liberation Analyser. Polished sections were prepared from 171 samples collected from two boreholes, for the in-situ examination of platinum group minerals (PGM). PGM and gold minerals encountered include maslovite (PtBiTe, 32 area% of total PGM), kotulskite (Pd(BiTe), 17?%), isoferroplatinum (Pt₃Fe, 15?%), sperrylite (PtAs₂, 11?%), cooperite (PtS, 5?%), moncheite (PtTe₂; 5?%), electrum (AuAg; 5?%), michenerite (PdBiTe; 3?%), Pd alloys (Pd, Sb, Sn; 3?%), hollingworthite ((Rh,Pt)AsS; 2?%), as well as minor (all <1 area% of total PGM) merenskyite (PdBiTe₂), laurite (RuS₂), rustenburgite (Pt_0.4Pd_0.4Sn_0.2), froodite (PdBi₂), atokite (Pd_0.5Pt_0.3Sn_0.2), stumpflite (PtSb), plumbopalladinite (Pd₃Pb₂), and zvyagintsevite (Pd₃Pb). An observed association of all PGM with base metal sulfides (BMS), and a pronounced association of PGE tellurides, arsenides and Pd&Pt alloys with secondary silicates, is consistent with the remobilisation and recrystallisation of some of the PGM’s during hydrothermal alteration and serpentinisation subsequent to their initial (primary) crystallisation from BMS (e.g. Godel et al. J Petrol 48:1569–1604, 2007; Hutchinson and McDonald Appl Earth Sci (Trans Inst Min Metall B) 114:B208–224, 2008).     

Dissociation of CAS phase in the uppermost lower mantle

The high-pressure stability limit of calcium aluminosilicate (CAS) phase has been examined in its end-member CaAl₄Si₂O₁₁ composition at 18–39 GPa and 1,670–2,300 K in a laser-heated diamond-anvil cell (LHDAC). The in-situ synchrotron X-ray diffraction measurements revealed that the CAS phase decomposes into three-phase assemblage of cubic Al-bearing CaSiO₃ perovskite, Al₂O₃ corundum, and SiO₂ stishovite above 30 GPa and 2,000 K with a positive pressure–temperature slope. Present results have important implications for the subsolidus mineral assemblage of subducted sediment and the melting phase relation of basalt in the lower mantle.     

Seawater-peridotite interaction at 300°C and 500 bars: implications for the origin of oceanic serpentinites

An experiment has been performed reacting seawater with fresh peridotite (80% olivine, Fo₉₀ and ～- 15% enstatitic orthopyroxene En₉₅ and minor clinopyroxene and spinel) at 300°C, 500 bars and water/rock mass ratio of 20. The duration of the experiment was approximately 1500 hr.Seawater chemistry was appreciably modified during the experiment. Mg, Ca, Sr, SO₄ and H₂O were removed, while H₂S_(aq), Fe, Mn and Zn were added. H₂S_(aq) resulted from the inorganic reduction of seawater SO₄. pH was initially acid (2.8), but then rose slowly to a value of 5.2. The aqueous concentrations of Na, K, Cl and boron (B) changed little from that in seawater prior to reaction. However, as the solution was cooled to room temperature at the end of the experiment, the B concentration decreased. This suggests that the B content of oceanic serpentinites may be the result of retrograde reactions between a previously serpentinized body and ‘cold’ seawater.The primary minerals in the peridotite were replaced to varying degrees by serpentine (lizardite), magnetite. Mg-hydroxysulfate, anhydrite and possibly pyrite and sphalerite. Mg-hydroxysulfate and much anhydrite dissolved on quench.The alteration mineral assemblage generated during this experiment is consistent with that predicted from equilibrium phase relations and is similar in chemical composition, mineralogy and paragenesis to that reported for oceanic serpentinites.     

Mineral CuFe<Subscript>2</Subscript>S<Subscript>4</Subscript> from sulfide Copper–Nickel ores of the Lovnoozero deposit,Kola Peninsula

The unnamed mineral CuFe₂S₄ has been found from sulfide Cu–Ni ores of the Lovnoozero deposit in the Kola Peninsula, Russia. It occurs in norite composed of orthopyroxene (bronzite), Ca-rich plagioclase (66% An), pargasite, and phlogopite. The last two minerals are replaced by talc, chlorite and carbonates. Monoclinic pyrrhotite, pentlandite, chalcopyrite, and pyrite are associated ore minerals. Phase CuFe₂S₄ is enclosed predominantly in chalcopyrite, probably replacing it, and occurs in later carbonate veinlets together with redeposited sulfides. It is light yellow with a brownish tint and metallic luster. The Mohs hardness is 5–5.5; VHN 654 ± 86 kgs/mm². Density (calc.) = 4.524 g/cm³. The mineral is anisotropic, internal reflections are absent. Reflectance values (λ, nm R′ _g and R′ _p %) are: 440 30.3 29.5, 500 43.7 42.8, 560 50.9 49.6, 620 52.4 51.2, 640 52.6 51.4, 680 52.8 51.6, 700 52.7 51.4. CuFe₂S₄ is monoclinic, a = 6.260(4), b = 5.39(1), c = 13.19(1) Å, β = 94.88(7)°, V = 443(1) ų, Z = 4. The strongest reflections in the powder diffraction pattern are [d, Å (I) (hkl)]: 4.150 (10) (012), 3.559 (4) (\(11\bar 2\)), 3.020 (4) (\(10\bar 4\)), 2.560 (3) (\(21\bar 2\)), 2.500 (3) (\(10\bar 5\)), 2.340 (3) (\(12\bar 2\)), 1.817 (3) (215), 1.489 (3) (402). The chemical composition is as follows, wt %: 20.44 Cu, 35.85 Fe, 0.65 Ni, 0.14 Co, 43.15 S, total is 100.23. The empirical formula calculated on the basis of 7 atoms is Cu_0.969(Fe_1.934Ni_0.034Co_0.007)_1.975S_4.056. According to its mode of occurrence, the mineral was formed as a result of low temperature processes involving metamorphic hydrothermal solutions.     

Deformation history of the Paleoproterozoic Liaohe assemblage in the eastern block of the North China Craton

The Paleoproterozoic Liaohe assemblage and associated Liaoji granitoids represent the youngest basement in the Eastern Block of the North China Craton. Various structural elements and metamorphic reaction relations indicate that the Liaohe assemblage has experienced three distinct deformational events (D₁ to D₃) and four episodes of metamorphism (M₁ to M₄). The earliest greenschist facies event (M₁) is recognized in undeformed or weakly deformed domains wrapped by the S₁ schistosity, suggesting that M₁ occurred before D₁. The D₁ deformation produced small, mostly meter-scale, isoclinal and recumbent folds (F₁), an associated penetrative axial planar schistosity (S₁), a mineral stretching lineation (L₁) and regional-scale ductile shear zones. Concurrent with D₁ was M₂ metamorphism, which occurred before D₂ and produced low- to medium-pressure amphibolite facies assemblages. Regionally divergent motion senses reflected by the asymmetric F₁ folds and other sense-of-shear indicators, together with the radial distribution of the L₁ lineation surrounding the Liaoji granitoids, imply that D₁ represents an extensional event. The D₂ deformation produced open to tight F₂ folds of varying scales, S₂ axial crenulation cleavages and ENE-NE-striking thrust faults, involving broadly NW–SE compression. Following D₂ was M₃ metamorphism that led to the formation of sillimanite and cordierite in low-pressure type rocks and kyanite in medium-pressure rocks. The last deformational event (D₃) formed NW-WNW-trending folds (F₃), axial planar kink bands, spaced cleavages (S₃), and strike–slip and thrust faults, which deflect the earlier D₁ and D₂ structures. D₃ occurred at a shallow crustal level and was associated with, or followed by, a greenschist facies retrograde metamorphic event (M₄).The Liaohe assemblage and associated Liaoji granitoids are considered to have formed in a Paleoproterozoic rift, the late spreading of which led to the occurrence of the early extensional deformation (D₁) and the M₁ and M₂ metamorphism, and the final closing of which was associated with the D₂ and D₃ phases of deformation and M₃ and M₄ metamorphism.     

Bortnikovite,Pd<Subscript>4</Subscript>Cu<Subscript>3</Subscript>Zn,a new mineral species from the unique Konder placer deposit,Khabarovsk krai,Russia

Bortnikovite, a new mineral species that is an intermetallic compound of Pd, Cu, and Zn with the simplified formula Pd₄Cu₃Zn has been detected at the unique Konder placer deposit in the Ayan-Maya district, Khabarovsk krai. The primary source of this placer is a concentrically zoned alkaline ultramafic massif. The X-ray diffraction pattern is indexed on the assumption of a tetragonal unit cell: a = 6.00 ± 0.02 Å and c = 8.50 ± 0.03 Å, V = 306 ± 0.01 ų, Z = 3, probable space group P4/mmm. The calculated density is 11.16 g/cm³; the mean microhardness VHN is 368 kg/mm². In reflected light, the new mineral is white with a slight grayish beige tint; bireflectance, anisotropy, and internal reflections are not observed. The reflectance spectrum belongs to the concave group of the anomalous type. The measured values of reflectance are as follows: 56.9 (470 nm), 61.7 (546 nm), 63.4 (589 nm), and 65.4% (650 nm). The new mineral is intergrown with isoferroplatinum, titanite, perovskite, V-bearing magnetite, bornite, and chlorite. The origin of bortnikovite is related to the effect of alkaline fluid on ultramafic rocks. The new mineral is named in honor of Professor Nikolai Stefanovich Bortnikov, a prominent mineralogist and researcher of ore deposits and a corresponding member of the Russian Academy of Sciences. Bortnikovite is the first platinum group mineral that contains Zn as a major mineralforming element.     

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.     

Component migration patterns during the formation of a metamorphic layering, Mount Franks area, Willyama Complex, N.S.W., Australia

Mineral shapes, sizes and proportions in mica rich (M) and quartz-mica (QM) domains of an S₄ metamorphic layering have been compared in two mutually perpendicular orientations with shapes, sizes and proportions in mildly crenulated S₂ enclaves preserved within a rock from part of the Willyama Complex, N.S.W., Australia. The study has shown that data from two orientations are necessary to place constraints on the movement of mineral components dissolved in solution during formation of the layering. Comparison of mineral data has shown that SiO₂ has been dissolved from quartz grains in both M and QM domains. The SiO₂ lost from M domains has not migrated into QM domains. Measurements have also shown that biotite has undergone less solution than quartz. Most of the biotite components have probably undergone reaction to form probable syn—S₄ muscovite and chlorite. The muscovite-forming reaction requíres some silica on the lefthand side of the reaction, probably more than can be supplied by the chlorite-forming reaction. Some of this extra silica was supplied from dissolved quartz grains. However, only a small amount is needed for this purpose and most of the SiO₂ has left the system. Some syn—S₄ muscovite may have formed in M domains where it lies within the crenulated S₂. Direct evidence for its growth is hard to find.