Geochemistry and mineralogy of bentonites from Ishirini (Libya)

Smectites from the Ishirini bentonite deposit (Libya) were analysed for their oxygen and hydrogen isotopic ratios. Based on published isotopic fractionation data, the results indicate a predominantly meteoric origin of the fluids responsible for the transformation of pyroclastic rocks to bentonite at temperatures ranging from 30 to 90 °C. The thermal effect of the subsequent emplacement of volcanic intrusions was further evaluated by a detailed study of δ¹⁸O isotopic composition of smectites and fluid inclusions in quartz separated from silicified rings produced by the thermal action of a basalt dike. Five different groups of fluids were distinguished based on salinity and homogenization temperatures.

The contact zone of bentonite affected by high concentrated saline solution exhibit mineralogical changes. High salinity and high temperature also remarkably influence the technical parameters of bentonites and reduce, for example, the cation exchange capacity (CEC) or microporosity.     

Geochemistry and mineralogy of platinum group element in ores of the Kingash deposit,Eastern Sayan,Russia

The paper discusses the results of studying the contents of platinum group elements (PGE) and platinum group minerals (PGM) in ores of the Kingash deposit. The bulk of PGE has been established as concentrated in disseminated sulfide chalcopyrite–pyrrhotite–pentlandite ore and is represented by palladium bismuth–tellurides. During melt differentiation, the content and relationship of PGE are changed; the Pd/Pt value increases (up to 1.9 and 4.2 in dunite and wehrlite, respectively) with decreasing Mg number. The distribution of PGE, sulfur, and REE in various ore types suggests two formation mechanisms of high-grade ores: (1) the product of liquid immiscibility and gravity separation at the early magmatic stage and (2) involvement of the residual melt saturated in volatiles, which contributed to transportation and segregation of PGE at the late magmatic stage. The evolution of the ore system of the Kingash massif is characterized by sequential enrichment of PGM in Ni from high-Mg to low-Mg rocks similarly to sulfide minerals of disseminated ore. The criteria for ore content in utramafics of the Kansk block have been identified based on compared ore element and PGE concentrations in ultramafic rocks of the Kingash and Idar complexes.     

Material composition and geochemical characteristics of ores of the Malinovskoe gold-ore deposit (Primorskii Krai,Russia)

The mineral composition and geochemical characteristics of the ores of the Malinovskoe gold-ore deposit are studied by the data from mining works (ditches, cleanings, and boreholes). It is found that the ore–magma system of the deposit was formed in several stages of mineralization characterized by two phases of magmatism differing in age. In terms of the set of features (the geological–structural position of the deposit, as well as the material composition and geochemical characteristics of the ores), the deposit is attributed to the gold–tourmaline type of mineralization associated spatially and genetically with the “raremetal” granitoid magmatism. This type has not previously been found in Primorskii Krai. The studies of the material composition and geochemical characteristics of the ores allow us to ascertain the correlations between the elements along with the reasons of their origination. By analogy with other gold-ore formations of the Russian Far East, the mineralogical and geochemical model of the deposit is developed (Be–Sn–Cr–Ba–Au–Cu–Mo–Pb–V–Ti–Co–W–Ag–Bi–Ni–Mn–Sr–Zn–Sb–As modeling element series of vertical zoning), which enables us to estimate the levels of the erosion section of the ore bodies and to evaluate their prospects. It is found that the most productive associations in the deposit are the gold–bismuth geochemical association (Au–Ag–Bi–Cu–As–Co) and, to a lesser degree, the gold–tungsten association (W–Au–Ag–Cu–Bi–As).     

Geochemistry and mineralogy of arsenic in (natural) anaerobic groundwaters

Here new data from field bioremediation experiments and geochemical modeling are reported to illustrate the principal geochemical behavior of As in anaerobic groundwaters. In the field bioremediation experiments, groundwater in Holocene alluvial aquifers in Bangladesh was amended with labile water-soluble organic C (molasses) and MgSO₄ to stimulate metabolism of indigenous SO₄-reducing bacteria (SRB). In the USA, the groundwater was contaminated by Zn, Cd and SO₄, and contained <10 μg/L As under oxidized conditions, and a mixture of sucrose and methanol were injected to stimulate SRB metabolism. In Bangladesh, groundwater was under moderately reducing conditions and contained ∼10 mg/L Fe and ∼100 μg/L As. In the USA experiment, groundwater rapidly became anaerobic, and dissolved Fe and As increased dramatically (As > 1000 μg/L) under geochemical conditions consistent with bacterial Fe-reducing conditions. With time, groundwater became more reducing and biogenic SO₄ reduction began, and Cd and Zn were virtually completely removed due to precipitation of sphalerite (ZnS) and other metal sulfide mineral(s). Following precipitation of chalcophile elements Zn and Cd, the concentrations of Fe and As both began to decrease in groundwater, presumably due to formation of As-bearing FeS/FeS₂. By the end of the six-month experiment, dissolved As had returned to below background levels. In the initial Bangladesh experiment, As decreased to virtually zero once biogenic SO₄ reduction commenced but increased to pre-experiment level once SO₄ reduction ended. In the ongoing experiment, both SO₄ and Fe(II) were amended to groundwater to evaluate if FeS/FeS₂ formation causes longer-lived As removal. Because As-bearing pyrite is the common product of SRB metabolism in Holocene alluvial aquifers in both the USA and Southeast Asia, it was endeavored to derive thermodynamic data for arsenian pyrite to better predict geochemical processes in naturally reducing groundwaters. Including the new data for arsenian pyrite into Geochemist’s Workbench, its stability field completely dominates in reducing Eh–pH space and “displaces” other As-sulfides (orpiment, realgar) that have been implied to be important in previous modeling exercises and reported in rare field conditions.     

Geochemistry and mineralogy of platinum-group elements at Hartley Platinum Mine,Zimbabwe

The behaviour of platinum-group elements (PGE) in the exogenic cycle was examined in profiles of oxidized Main Sulfide Zone (MSZ) ores, in which the general metal distribution patterns of the pristine MSZ are grossly preserved. However, at similar Pt grades, significant proportions of Pd have been lost from the system. This indicates that Pd is more mobile than Pt and is dispersed in the supergene environment. Sperrylite and cooperite/braggite are stable in the oxidized MSZ. In contrast, the (Pt,Pd)-bismuthotellurides, common in pristine MSZ ores, have disintegrated, and ill-defined (Pt,Pd)-oxides or (Pt,Pd)-hydroxides have formed. The assemblage of detrital PGM present in the Makwiro River close to the Hartley Platinum Mine indicates further mineralogical changes. Sperrylite largely remains stable whereas most cooperite/braggite grains have been partly altered or completely destroyed. Grains of Pt-Fe alloy are ubiquitous in the alluvial sediments. Most likely, these grains are neo-formations that formed either from pre-existing, unstable PGM or via a solution stage under low-temperature conditions.     

New Data on the Geochemistry of Mississippi-Type Ores at the Sardana Deposit (Northeastern Russia)

New data obtained using a modern analytical technique on the geochemistry and conditions of the formation of Mississippi-type ores at the Sardana deposit are presented. Comparative analysis related to other deposits of the same type was carried out. The geochemical data point to a considerable role of metamorphism of the enclosing carbonate–terrigenous masses in ore formation at the deposit.     

Geochemistry, mineralogy, and technological properties of the main Stephanian (Carboniferous) coal seams from the Puertollano Basin, Spain

This study is focused on the occurrence and distribution of mineral matter and major and trace elements in the high volatile bituminous coal from Puertollano (south-central Spain). The relationship between ash behaviour and inorganic composition, as well as the possible formation of fouling and slagging deposits in boilers during the conversion process, were investigated. The Puertollano coals do not exhibit plastic properties, despite their rank, probably because of their high ash and inertinite contents.The Puertollano coal has medium to low total S content (0.48% to 1.63% db, with a mean of 1.0% db) and is characterised by relatively high contents of Si, Pb, Sb, and Cs. Some elements such as As, Cd, Co, Cr, Cu, Ge, Li, Mn, Ni, W, and Zn are also present in relatively high contents. The enrichment in a number of heavy metals could be attributed to the common sulphide ores occurring near the Puertollano coal deposit.The following trace elements affinities are deduced: (a) sulphide affinity: As, Co, Cd, Cu, Ni, Sb, Tl, and Zn; (b) aluminum–silicate affinity: K, Ti, B, Co, Cr, Cs, Cu Ga, Hf, Li, Nb, Rb, Sn, Ta, Th, V, Zr, and LREE; (c) Carbonate affinity: Ca, Mg, Mn, and B; (d) organic affinity: B.The very high Si levels and the anomalous enrichment in Cs, Ge, Pb, Sb, and Zn shown by the Puertollano coals account for the high contents of these elements in the Puertollano fly ash when compared with the other Spanish coal fly ashes.The chemical composition of the high temperature ash (HTA) is consistent with the trend shown by the ash fusion temperatures (AFT) and also with the predictive indices related to slagging and fouling propensities. Thus, the ash fusion temperatures increase with high values of Al₂O₃ as well as with the decrease in Fe₂O₃, CaO, and MgO.     

Geochemistry and mineralogy of surface pyritic tailings impoundments at two mining sites of the Iberian Pyrite Belt (SW Spain)

Two pyritic tailings impoundments located in two mining areas of the Iberian Pyrite Belt (Cueva de la Mora and Minas de Ríotinto-Zarandas) were selected to asses their potential environmental impact. Mineralogical (XRD diffraction study), physico-chemical characterization (colour, particle size, pH, acid–base account, total Fe, As, Cu, Pb and Zn) as well as a speciation study (by means of a seven-step sequential extraction procedure) were performed in superficial (0–20 cm) tailings samples. Arsenic and metal contents in soils around the tailings impoundments were also studied. Zarandas dam, a reclaimed impoundment, which has been limed, partially topsoiled and planted, has supported and allowed the growth of pine trees and other plants for many years. The surface of this impoundment can be considered very acid but nonacid forming. Although total As and metal concentrations were relatively high, it is not possible to conclude that the Zarandas tailings have polluted the surrounding soils. Tailings in Cueva de la Mora showed high total and easily mobilizable concentration of toxic elements. The net neutralization potential was strongly negative as a consequence of the acid generation caused by the sulphide oxidation, the presence of secondary acid-generating minerals and the absence of neutralizing materials. Coquimbite and rhomboclase efflorescences formed during the Mediterranean dry summers on the surface of this impoundment contained very high levels of soluble As, Cu and Zn that were easily dissolved and released to the running water in the first rains of autumn.     

Hydrochemical models of the sulphidic tailings dumps at Matchless (Namibia) and Selebi-Phikwe (Botswana)

The sulphidic tailings dumps at Matchless (Namibia) and Selebi-Phikwe (Botswana) are located in a similar semiarid environment but have a contrasting mineralogical composition. The Matchless tailings are pyrite-rich, whereas the Selebi-Phikwe tailings are dominated by pyrrhotite. Hydrochemical models are established with computer codes for water-balance, sulphide oxidation rate and hydrochemical equilibrium calculations. The data input is based on detailed mineralogical, chemical and kinetic investigations carried out on the core of boreholes drilled in 2000 and 2003. The oxidation of pyrrhotite proceeds at a much faster rate than the oxidation of pyrite. The PYROX code, which is used for kinetic calculations, can take these differences into account by applying different oxide-coating diffusion coefficients (D₂) for pyrrhotite and pyrite. Humidity-cell testing is widely used to predict the post-mining composition of drainage water in humid climates. However, the semiarid conditions at Matchless and Selebi-Phikwe only allow a minimal water flux within the dump. Under such conditions, humidity-cell testing is likely to overestimate the seepage-water pH. This is suggested by the hydrochemical equilibrium calculations for the post-mining period at Selebi-Phikwe, which predict a seepage-water pH about one unit lower than the pH at the end of the 26-weeks humidity-cell testing period. The acidity of the seepage water can be reduced by about half a pH unit, if an oxygen barrier below the evaporation zone is installed. A clay layer 0.5 m thick covered by >1.5 m tailings represents the optimal design for a wet barrier. All three computer codes used for water-balance calculations (HELP3, UNSAT-H and HYDRUS-1D), predict >85% average water saturation for such a layer, which diminishes the diffusion of oxygen into the pile and production of SO₄⁻² and H⁺. The alternative design for a dry barrier consists of a vegetated silt layer 1 m thick on top of the tailings. This barrier does not significantly influence the diffusion of oxygen although it reduces the net infiltration to ≤11 mm/year.     

The Vorontsovskoe Au-Hg-As ore deposit (Northern Urals,Russia): Geological setting,ore mineralogy,geochemistry, geochronology and genetic model

The large Vorontsovskoe Au-Hg-As deposit in the Urals is located in the exocontact of the Early Devonian Auerbah gabbro-diorite-granodiorite massif, which intrudes volcano-sedimentary rocks. The orebodies are confined to a tectonic contact of calcareous and tuffaceous rocks. They are composed of 6 types of disseminated ores, but the main reserves of gold are associated with the following ore types: gold-pyrite-arsenopyrite in altered tuffaceous rocks, pyrite-realgar ores in limestone breccia with a carbonate-volcanogenic cement, and gold-oxide-clay from regolith with residual gold. Early ore associations have been formed at 450–300 °C, whereas the late ores have been formed at lower temperature of 260–110 °C. We propose a model for the genesis of the Vorontsovskoe deposit based on synchronicity of mineralization with the formation of the Auerbah volcano-plutonic complex. The Ar-Ar age of hydromica from the gold-arsenopyrite association is 391.1 ± 4.9 Ma, which coincides with the age of igneous rocks of the Auerbah complex. The main sources of water and carbon dioxide were composed of the fluid derived from the magma chamber and the metamorphic water equilibrated with carbonate sedimentary rocks. Magmatic fluid dominated during the development of skarns, jasperoids and quartz veins, whereas metamorphic water was dominant during quartz-sericite alteration of volcano-sedimentary rocks and calcareous breccias. The bulk of the sulfur was supplied by a deep magma reservoir, however this source prevailed only during skarn ore formation. The mixing between deep-sourced sulfur and sedimentary or biogenic sulfur was established for other ore types. Gold and other ore components were possibly introduced during the volcanic and intrusive activity and also extracted from host sedimentary rocks.     

Geochemistry of mineral water and gases of the Razdolnoe Spa (Primorye,Far East of Russia)

New isotopic and chemical data on the sodium bicarbonate water and associated gases from the Razdolnoe Spa located in the coastal zone of Primorsky Kray of the Russian Far East, together with previous stable isotope data (δ¹⁸O, δD, δ¹³C), allow elucidation of the origin and evolution of the groundwater and gases from the spa. The water is characterized by low temperature (12 °C), TDS – 2.5–6.0 g/L, high contents of B (∼5 mg/L) and F (4.5 mg/L) and low contents of Cl and SO₄. Water isotopic composition indicates its essentially meteoric origin which may comply with an older groundwater that was recharged under different (colder) climatic conditions. Major components of bubbling gases are CH₄ (68 vol%), N₂ (28%) and CO₂ (4%). The obtained values δ¹³C and δD for CO₂ and CH₄ definitely indicate the marine microbial origin of methane. Thus the high methane content in the waters relates to the biochemical processes and presence of a dispersed organic matter in the host rocks. Based on the regional hydrogeology and the geological structure of the Razdolnoe Spa, Mesozoic fractured rocks containing Na–HCO₃ mineral water and gases are reservoir rocks, a chemical composition of water and gases originates in different environmental conditions.     

东天山黄山-镜儿泉过铝花岗岩矿物学、地球化学及年代学研究

对东天山黄山-镜儿泉一带黄山南、镜儿泉、图拉尔根沟三个过铝花岗岩作了岩相学、矿物学、地球化学、sr-Nd同位素和锆石U-Pb年代学研究.锆石U-Pb LA-ICP-MS原位定年测得黄山南岩体结晶年龄为259.9±1.4Ma(MSWD=0.86),图拉尔根沟岩体结晶年龄为275.4±8.3Ma(MSWD=29),均侵位于二叠纪碰撞后伸展环境.三个过铝花岗岩均具有低锶同位素初始比值(Isr=0.6969～0.70396)、高εNd(t)值( 5.5～ 7.2)以及年轻的亏损地幔单阶段模式年龄(tDM=0.48～0.56Ga),表明其岩浆源区均为来源于亏损地幔的新生地壳岩石.这种新生地壳岩石可能为偏酸性的火山岩.三个岩体的矿物学和地球化学可分为两类:一类以黄山南白云母花岗岩为代表,为强过铝花岗岩(A/CNK>1.1),强烈亏损Ba、sr和Ti而富集Cs、Rb和K,具有高的Rb/sr(2.03～14.5)和Al2O3/TiO2(110～1592),低的Nb/Ta(3.24～6.76)比值,其稀土元素配分曲线呈"V"字形,显示强烈铕亏损(Eu/Eu*=0.04～0.55),表明这类岩体的直接源岩以泥质岩为主.另一类以图拉尔根沟二云母花岗岩为代表,为弱过铝(1   

Platinum group elements zoning and mineralogy of chromitites from the cumulate sequence of the Nurali massif (Southern Urals, Russia)

The Nurali lherzolite massif is one of the dismembered ophiolite bodies associated with the Main Uralian Fault (Southern Urals, Russia). It comprises a mainly lherzolitic mantle section, an ultramafic clinopyroxene-rich cumulate sequence (Transition Zone), and an amphibole gabbro unit.The cumulate section hosts small chromitite bodies at different stratigraphic heights within the sequence. Chromitite bodies from three different levels along a full section of the cumulate sequence and two from other localities were investigated. They differ in the host lithology, chromitite texture and composition, and PGE content and mineralogy. Chromitites at the lowest level, which are hosted by clinopyroxenite, form cm-scale flattened lenses. They have high Cr# and low Mg# chromites and are enriched in Pt and Pd relative to Os and Ir. At a higher, intermediate level, the chromitites are hosted by dunite. They form meter thick lenses, contain low Cr# and high Mg# chromites, have high PGE contents (up to 26,700 ppb), and are enriched in Os, Ir and Ru relative to Pt and Pd, reflecting a mineralogy dominated by laurite–erlichmanite and PGE–Fe alloys. At the highest level are chromitites hosted by olivine–enstatite rocks. These chromitites have high Cr# and relatively low Mg# chromites and very low PGE content, with laurite as the dominant PGE mineral.The platinum group minerals (PGMs) show extreme zoning, with compositions ranging from erlichmanite to almost pure laurite and from Os-rich to Ru-rich alloys, with variable and irregular zoning patterns.Two chromitite bodies up to 6 km from the main sequence can be correlated with the latter based on geochemistry and mineralogy, implying that the variations in chromitite geochemistry are due to processes that operated on the scale of the massif rather than those that operated on the scale of the outcrop.Pertsev et al. [Pertsev, A.N., Spadea, P., Savelieva, G.N., Gaggero, L., 1997. Nature of the transition zone in the Nurali ophiolite, Southern Urals. Tectonophysics 276, 163–180.] propose that the Transition Zone formed by solidification of a series of small magma bodies that partially overlapped in time and space. The magmas formed by successive partial melting of the underlying mantle. We suggest that this process determined the changing PGE geochemistry of the successive batches of magma. The PGE distribution fits a model of selected extraction from the mantle, where monosulphide solid solution–sulphide liquid equilibrium was attained until complete melting of the monosulphide solid solution. Later and localized variations in fS₂ resulted in the formation of different PGMs with complex zoning patterns.     

Platinum-group Element Geochemistry of Magnetite from Porphyry-Cu-Mo Deposits and their Host Rocks (Siberia,Russia)

The concentrations of platinum-group elements (PGE) have been analyzed in primary magmatic magnetite samples from the Zhireken,Shakhtama and Aksug porphyry Cu-Mo deposits (Siberia,Russia) by laser abla...     

Geology and mineralogy of the Alakha spodumene granite porphyry deposit,Gorny Altai,Russia

The Alakha lithium–tantalum deposit in the southern Altai, Russia, is represented by a stock of spodumene-bearing granite porphyry localized in the Kalba–Narym–Koktogai lithium–tantalum rare-metal granitic belt, unique in extent (more than 1000 km). This belt is a part of the Altai accretionary–collisional system. Judging from forecasting, the Alakha deposit can be regarded as an uneroded proxy of a pegmatite body both in dimensions and mean Li₂O and Ta₂O₅ contents (0.98 wt % and 114 ppm, respectively); however, the oregenerating potential of this deposit remains insufficiently studied and had not yet been claimed. In this paper, we attempt to fill this gap with a detailed mineralogical study, which allows us to provide insights into the crystallization of Li-bearing high-silicic magma and redistribution of components during magmatic and postmagmatic processes. Accessory mineral assemblages in muscovite–spodumene–K-feldspar granite porphyry and muscovite albitite—the main petrographic rock varieties of the Alakha stock—turned out to be almost identical. A significant similarity in the chemistry of major rock-forming minerals is established for spodumene granite porphyry of the Alakha stock and spodumene pegmatites from large deposits, which makes it possible to suggest that they are close in the petrogenetic mechanism of their formation. The mineral assemblages of muscovite albitite in the apical portion of the Alakha stock are connected by gradual transition with those of spodumene granite porphyry. Such a transition is caused by postmagmatic metasomatic alteration of the latter.     

Economic minerals of the Kovdor baddeleyite-apatite-magnetite deposit,Russia: mineralogy,spatial distribution and ore processing optimization

The comprehensive petrographical, petrochemical and mineralogical study of the Kovdor magnetite-apatite-baddeleyite deposit in the phoscorite–carbonatite complex (Murmansk Region, Russia) revealed a spatial distribution of grain size and chemical composition of three economically extractable minerals — magnetite, apatite, and baddeleyite, showing that zonal distribution of mineral properties mimics both concentric and vertical zonation of the carbonatite-phoscorite pipe.The marginal zone of the pipe consists of (apatite)-forsterite phoscorite carrying fine grains of Ti–Mn–Si–rich magnetite with ilmenite exsolution lamellae, fine grains of Fe–Mg-rich apatite and finest grains of baddeleyite, enriched in Mg, Fe, Si and Mn. The intermediate zone accommodates carbonate-free magnetite-rich phoscorites that carry medium to coarse grains of Mg–Al-rich magnetite with exsolution inclusions of spinel, medium-grained pure apatite and baddeleyite. The axial zone hosts carbonate-rich phoscorites and phoscorite-related carbonatites bearing medium-grained Ti–V–Ca-rich magnetite with exsolution inclusions of geikielite–ilmenite, fine grains of Ba–Sr–Ln-rich apatite and comparatively large grains of baddeleyite, enriched in Hf, Ta, Nb and Sc. The collected data enable us to predict such important mineralogical characteristics of the multicomponent ore as chemical composition and grain size of economic and associated minerals, presence of contaminating inclusions, etc. We have identified potential areas of maximum concentration of such by-products as scandium, niobium and hafnium in baddeleyite and REEs in apatite.     

俄罗斯勘察加半岛热泉的地球化学和微生物学

勘察加半岛位于欧洲板块、北美板块和太平洋板块交汇的过渡带上,是世界火山活动最活跃的地区之一.其众多的热液系统不断的向地表释放地热气体和流体.以N2和CO2为主的地热气体也经常含有高浓度的H2,CH4和H2S.大气水和熔岩水构成了勘察加热泉水的主要源,水体温度从20 ℃到＞90 ℃不等.水化学性质变化同样显著,pH范围从3.1到9.8.热泉水溶解盐以氯化钠为主,同时包括K+,H3BO3,H4SiO4,Ca2+和SO42-等其他多种溶解组分.此区域也有以直链烷烃为主的石油形成.从勘察加的热泉系统中已分离出至少24种嗜热微生物.尽管其中大多数是异养微生物,但根据其生存环境的特点,自养微生物在热泉系统中可能同样很多.这些微生物对碳、硫和铁在热液系统中的生物地球化学循环有着非常重要的作用.目前,非培养的方法和生物定量的手段已用来研究勘察加热泉中微生物生态及其所具有的生物地球化学功能.     

Geochemistry and mineralogy of lavas from the Arakapas Fault Belt,Cyprus: Consequences for magma chamber evolution

Résumé Résumé L'étude géochimique des laves dans la zone d'Arakapas (AFB) a permis de proposer un modèle génétique pour la formation des laves et des cumulats qui s'est déroulée dans un seul site géotectonique. Cinq types de lave ont été définis dans l'AFB, un dans la séquence axiale (AS) et quatre dans les laves en coussin supérieures (UPL) formés à partir d'un manteau très déprimé dont le degré d'appauvrissement s'est accru avec le temps. La modélisation des processus de fusion partielle et de cristallisation fractionnée implique des coefficients de partage élevés pour Mg et Cr et faibles pour V compatibles avec une fugacité d'oxygène élevée dans la source.Dans les différents types de lave, la cristallisation plus ou moins précoce du plagioclase, du clinopyroxène ou de l'orthopyroxène après l'olivine témoigne de l'existence de magmas parentaux distincts qui ont alimenté des chambres magmatiques évoluant en système fermé. La disparition des grandes chambres magmatiques d'où ont été issues les laves de type A a eu lieu en fin de formation de l'AS. Les chambres magmatiques plus petites liées aux UPL ont été détruites à différents stades de leur évolution.

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Geochemistry and mineralogy of lavas from the Arakapas Fault Belt, Cyprus: Consequences for magma chamber evolution

Summary The results of geochemical investigations in the Arakapas Fault Belt (AFB) in the Cyprus ophiolite are discussed to provide a comprehensive model for the genesis of the ophiolitic intrusive and extrusive rocks which occur in a single but evolutive tectonic environment.On the basis of field and petrographic criteria, five lava types are defined, one in the Axis Sequence (AS) and four in the Upper Pillow Lavas (UPL). The comparison between observed and calculated partial melting and fractional crystallization trends favors high D_Cr and D_Mg and low Dv consistent with high fO₂. Partial melting occurred in a depleted mantle after a prior melting event. The extent of mantle depletion varies with space and increases with time.Different crystallization orders in lavas reflect distinct parental magma compositions and the extent of pre-eruption fractionation dominated by wehrlitic crystallization in closed magma chambers. Long-lived magma chambers disappear at the end of the AS. Small magma chambers occurred during the formation of the UPI, and were destroyed at various degrees of evolution.

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With 6 Figures