The origin of major talc deposits in the Eastern Desert of Egypt: relict fragments of a metamorphosed carbonate horizon?

Detailed geochemical and mineralogical investigation of four talc deposits in the Eastern Desert of Egypt (Atshan, Abu Gurdi, Darhib and Kashira) suggests that the deposits form a distinct lithological unit within the Shadli metavolcanic rocks. The talc crystallized from the replacement of siliceous carbonate beds locally intercalated with clastic sediments. Th/Yb vs. Ta/Yb ratios of the rocks suggest that the sediments and the host volcanic rocks formed in an active continental margin (ACM) environment. Thus, the talc deposits may represent relict fragments of an ancient, regionally extensive carbonate horizon within the arc-related metavolcanics. The talc-rich rocks, which contain relict carbonate, serpentinized olivine and tremolite, have low (<3 wt%) Al₂O₃, Cr, Ni (<20 ppm), Co and Sc (<15 ppm) concentrations, precluding mafic or felsic igneous protoliths. The deposits were locally affected by contact metamorphism, giving rise to pyroxene-hornfels and granulite facies assemblages, and by regional metamorphism which produced greenschist-amphibolite grade assemblages. Disseminated sulfides commonly occur in the talc-tremolite-rich rocks (having low Al₂O₃ concentrations), suggesting that the metals were probably present in the original carbonate beds, but were remobilized and reconcentrated during the various metamorphic events.     

The deformation and recrystallization of biotite in the Woodroffe Thrust mylonite zone

The deformation and recrystallization microstructures in biotite from the Woodroffe Thrust mylonites are described and interpreted. The degree of strain causing recrystallization and the nucleation mechanisms differ across the mylonite zone. These differences are associated with the contrast in water content between the granulite and amphibolite facies felsic gneisses on either side of the zone. p]In moderately mylonitized granulite facies felsic gneisses (0.1–0.6% H₂O) subgrains form in intensely deformed host biotite and recrystallization mechanisms involve subgrain rotation both on host grain boundaries and associated with kink band bulge. In the amphibolite facies felsic gneisses (0.9–1.2% H₂O) the biotite recrystallizes by a mechanism involving localized internal kinking of the host and subsequent migration of high angle boundaries generated on the kink limbs. This combined with rotation due to the concurrent deformation generates high angle grain boundaries around the entire original kink limb and thus a new grain.     

The role of “excess” CO2 in the formation of trona deposits

The prevailing theory for the formation of trona [Na₃(CO₃)(HCO₃) · 2(H₂O)] relies on evaporative concentration of water produced by silicate hydrolysis of volcanic rock or volcaniclastic sediments. Given the abundance of closed drainage basins dominated by volcanics, it is puzzling that there are so few trona deposits and present-day lakes that would yield dominantly Na–CO₃ minerals upon evaporation. Groundwater in the San Bernardino Basin (southeastern Arizona, USA and northeastern Sonora, Mexico) would yield mainly Na–CO₃ minerals upon evaporation, but waters in the surrounding basins would not. Analysis of the chemical evolution of this groundwater shows that the critical difference from the surrounding basins is not lithology, but the injection of magmatic CO₂. Many major deposits of trona and Na–CO₃-type lakes appear to have had “excess” CO₂ input, either from magmatic sources or from the decay of organic matter. It is proposed that, along with the presence of volcanics, addition of “excess” CO₂ is an important pre-condition for the formation of trona deposits.     

Oxygen isotope geochemistry of the Granite Harbour Intrusives, Wilson Terrane, Northern Victoria Land, Antarctica

Summary The oxygen and strontium isotope compositions of the Cambro-Ordovician granitoids cropping out in the Wilson Terrane (Granite Harbour Intrusives–GHI) constrain the petrological evolution of the magmatism in Antarctica, related to the Ross Orogeny. The measured δ¹⁸O_WR values of these intrusives define three different compositional groups: the metaluminous rocks (MAG), with δ¹⁸O_WR ranging from 6.9 (olivine gabbro) to 11.4‰ (monzogranite); the unaltered peraluminous granites (PAG), having δ¹⁸O_WR values ranging from 10.6 to 13.2‰, and the foliated peraluminous leucogranites (SKG), characterised by δ¹⁸O_WR values above 14‰. The analysis of equilibrium mineral assemblages indicates that the high δ¹⁸O_WR values are magmatic and unaffected by low-temperature processes. A few peraluminous granites sampled in the vicinity of Cenozoic intrusions show anomalously low δ¹⁸O_WR, due to meteoric-hydrothermal alteration. The isotopic data indicate that the coeval and spatially related metaluminous mafic and felsic intrusives forming the GHI were not comagmatic: the mafic and intermediate rocks were likely derived from lower crustal contamination of a pristine basaltic magma; their δ¹⁸O_WR values were also increased during emplacement, due to the interaction with the adjacent ¹⁸O-rich hydrous felsic magmas (mixing). Oxygen isotope data indicate that the crustal sources producing the Granite Harbour intrusives were not homogeneous: the felsic metaluminous intrusives were produced by partial melting of fertile rock with possible igneous origin, whereas partial melting of a metapelitic source rock is claimed for the genesis of the peraluminous granites. Received February 9, 2001; revised version accepted August 10, 2001     

Comparative geochemistry of volcanics from rift valleys,transform faults and aseismic ridges

New chemical analyses and a review of published data show that there is a compositional diversity between volcanics of basaltic composition found in the M.A.R. rift valley, M.A.R. transform faults and aseismic ridges. The basaltic rocks from the M.A.R. transform faults are less mafic (depleted in olivine content) than those from the M.A.R. rift valley. The transform fault basalts have a higher range of TiO₂ content (1–4%), of Fe₂O₃+FeO content (8–14%) and a lower range of Cr content (50–500 ppm) and Ni content (50–300 ppm). The volcanics from aseismic ridges around the world are considered to be the more felsic types of the two provinces. They have a higher range of variation for their TiO₂ and Fe₂O₃+FeO (1.6–5%; 9–15%; respectively) and a lower range of variability for their Cr and Ni (<250 and 100 ppm respectively) than both the M.A.R. rift valley and transform fault volcanics.It is suggested that transform faults have, by faulting, exposed more fractionated types of basaltic rocks (may be as intrusives) than the rift valley volcanics. While aseismic ridges have undergone a greater degree of differentiation than both transform faults and rift valley volcanics.Contribution n 475 du Département Scientifique, Centre Océanologique de Bretagne Contribution No. 3803 of Woods Hole Oceanographic Institution (USA)     

Zr-rich accessory minerals (titanite, perrierite, zirconolite, baddeleyite) record strong oxidation associated with magma mixing in the south Peruvian potassic province

The Oroscocha Quaternary volcano, in the Inner Arc Domain of the Andean Cordillera (southern Peru), emitted peraluminous rhyolites and trachydacites that entrained decimetric to millimetric lamprophyric blobs. These latter show kersantite modal compositions (equal proportion of groundmass plagioclase and K-feldspar) and potassic bulk-rock compositions (1<K₂O/Na₂O<2; 6.7–7.2 wt.% CaO). Kersantite blobs have shapes and microstructures consistent with an origin from a mixing process between mafic potassic melts and rhyolitic melts. Both melts did exchange their phenocrysts during the mixing process. In addition to index minerals of lamprophyres (Ba–Ti–phlogopite, F-rich apatite, andesine and Ca-rich sanidine), the groundmass of kersantite blobs displays essenite-rich diopside (up to 22 mol%), Ti-poor magnetite microlites, Ti-poor hematite microlites and a series of Ca–Ti–Zr- and REE-rich accessory minerals that have never been reported from lamprophyres. Titanite [up to 5.3 wt.% ZrO₂ and 5.2 wt.% (Y₂O₃ + REE₂O₃)] and Zr- and Ca-rich perrierite (up to 7.2 wt.% ZrO₂ and 10.8 wt.% CaO) predate LREE- and iron-rich zirconolite and Fe-, Ti-, Hf-, Nb- and Ce-rich baddeleyite (up to 5.3 wt.% Fe₂O₃, 3.2 wt.% TiO₂, 1.5 wt.% HfO₂, 1.2 wt.% Nb₂O₅, 0.25 wt.% CeO₂) in the crystallization order of the groundmass. Isomorphic substitutions suggest iron to occur as Fe³⁺ in all the accessory phases. This feature, the essenitic substitution in the clinopyroxene and the occurrence of hematite microlites, all indicate a drastic increase of the oxygen fugacity (from FMQ − 1 to FMQ + 5 log units) well above the HM synthetic buffer within a narrow temperature range (1100–1000 °C). Such a late-magmatic oxidation is ascribed to assimilation of water from the felsic melts during magma mixing, followed by rapid degassing and water dissociation during eruption of host felsic lavas. Thus, magma mixing involving felsic melt end-members provides a mechanism for mafic potassic melts to be oxidized beyond the HM synthetic buffer curve.     

Origin, weathering, and geochemical composition of loess in southwestern Hungary

Loess geochemistry generally reflects paleo-weathering conditions and it can be used to determine the average composition of the upper continental crust (UCC). In this study, major and trace element concentrations were analyzed on loess samples from southwestern Hungary to determine the factors influencing their chemical compositions and to propose new average loess compositions. All studied loess samples had nearly uniform chemical composition, suggesting similar alteration history of these deposits. Chemical Index of Alteration values (58–69) suggested a weak to moderate degree of weathering in a felsic source area. Typical non-steady state weathering conditions were shown on the Al₂O₃–CaO + Na₂O–K₂O patterns, indicating active tectonism of the Alpine–Carpathian system during the Pleistocene. Whole-rock element budgets were controlled by heavy minerals derived from a felsic magmatic or reworked sedimentary provenance. Geochemical parameters indicated that dust particles must have been recycled and well homogenized during fluvial and eolian transport processes.     

Experimental reactions of amphibolite with boron-bearing aqueous fluids at 200 MPa: implications for tourmaline stability and partial melting in mafic rocks

Reactions between hornblende-plagioclase amphibolite and acidic and alkaline B-bearing aqueous fluids have been investigated by experiments at 475°–600° C and 200 MPa. At 600° C, hornblende+calcic plagioclase react to form tourmaline+danburite+clinopyroxene+quartz in acidic fluids containing 0.5–1.0 wt% B₂O₃.Tourmaline is precipitated directly from acidic fluids, and the reaction is driven by neutralization of fluids by Na±Ca derived from the breakdown of reactant solids. The concentration of B₂O₃ in fluids needed to stabilize tourmaline increases as pH increases (above approximately 6.0), and tourmaline is unstable in alkaline fluids (pH > approximately 6.5–7.0) regardless of B concentration. In addition to acid-base relations, tourmaline stability is favored by comparatively higher activity coefficients for Al species in acidic fluids. The concentrations of Al and Si in fluid increase with alkalinity, with the eventual production of felsic borosilicate melts through partial melting of the plagioclase component of the amphibolite. In seeded experiments, tourmaline also contributes components to melt. Partial melting is evident in the range 500°–525° C at 200 MPa in experiments with 8wt% B₂O₃ in fluid as Na₂B₄O₇. The experimental results are applied primarily to metasomatic reactions between mafic rocks and borate fluids derived from granitic magmas, but tourmaline stability and partial melting in mafic regional metamorphic systems are also discussed briefly.     

The use of tourmaline in geochemical prospecting for gold and copper mineralization

Chemical composition, unit cell parameters, and trace elements of tourmalines from Mesozoic gold-quartz-sulphide and gold-bearing copper-porphyry ore-magmatic systems of the Trans-Baikal area and Mongolia show that they belong to the specific schorl-dravite highly ferruginous oxytourmaline series. They are low in alumina (Al₂O₃ = 16–33%) and have MgO contents (up to 10%) and Fe₂O₃ (1%). There is a direct correlation of unit cell parameters (a,c,V) with total iron, which permits composition estimates from X-ray diffraction analyses. As a rule, these tourmalines contain high concentrations of Au, Pb and Cu, which are mainly hosted by inclusions of native gold and ore minerals. The highest As abundances are contained in the tourmalines of the copper-porphyry field.Two trends of isomorphic replacement are related to increasing Fe content of oxyferruginous tourmalines:(1) “Acid leaching” trend (less ferruginous part of the series) Mg + Fe²⁺ + 4Al + 40 4Fe³⁺ + 2 + 4(OH,F); and (2) “conjugate deposition” trend Mg + 1.5Fe²⁺ + 1.5Al + 4(OH,F) 4Fe³⁺ + 4O.These features distinguish tourmalines from gold-bearing systems from schorl-dravites of tin and rare-metal deposits. They may be used in metallogenic analyses, interpretation of the origin of primary and secondary anomalies, and assessment of the type and zonation of ore fields.     

Holocene Siliceous Sediments in the Sea of Okhotsk

The mineral and chemical compositions and physical properties of diatomaceous clayey–siliceous sediments in the Sea of Okhotsk are studied. Absolute masses of silica accumulation are determined. Their compositional model based on the silica content is similar to that of Late Jurassic and Olenekian–middle Anisian cherts of the Sikhote Alin region. The thickness of the Holocene siliceous unit and the absolute mass of siliceous deposits depended on bioproductivity in the upper water column and the seafloor topography. Absolute masses of SiO₂ am (0.05–5.7 g cm^–2 ka^–1) and SiO₂ fr (0.5–11.6 g cm^–2 ka^–1) are minimal on seamounts and maximal in depressions near foothills. These values match absolute masses of SiO₂ fr accumulations in Triassic and Late Jurassic basins of the Sikhote Alin region (0.33–3 g cm^–2 ka^–1). Comparison of the composition and absolute masses of silica shows that Triassic and Late Jurassic siliceous sequences of Sikhote Alin could be accumulated in the marginal marine basin near a continent.     

Actual Problems of Prediction of Manganese Deposits in the Urals

Based on recent publications and our long-standing investigations, the most reasonable ways were proposed to obtain the manganiferous raw material for the Uralian metallurgic industry, which lost the traditional raw base (Ukrainian and Georgian deposits) after the USSR breakdown. The Urals is region is perspective for the discovery of two types of manganese deposits. (1) Insignificantly metamorphosed siliceous–carbonate ores with silica modulus M_Si (i.e., MnO : SiO₂) ranging from 1 to 2 and manganese content of 17–20%. The most promising are the areas with different-age, mainly carbonate rocks in the Urals (Northern and Polar) and Pai-Khoi regions. (2) Oxide, mainly pyrolusite–psylomelane ores with Mn content of 30–35% in the Meso–Cenozoic manganese hats developed in the Paleozoic manganiferous (volcanogenic–siliceous and carbonate–siliceous) rocks and noneconomic (small) deposits. The most promising areas are Late Cretaceous and Paleogene peneplains of the Southern Urals (Trans-Uralian and Zilair regions). It is necessary to intensify works on the improvement of concentration technique for manganese ores and to carry out the marketing study of the expediency of replacing imported manganiferous concentrates by those obtained from the Uralian ores.     

Identification of diagnostic geochemical alteration in the wallrocks of archean volcanic-exhalative massive sulfide deposits

The present investigation is concerned with the identification of diagnostic lithogeochemical alteration signatures around volcanic-exhalative massive sulfide deposits in the Superior Province, with the overall objective of deriving lithogeochemical criteria, applicable in the search for new deposits of this type.Previous work on these deposits has indicated that, in general, the footwall alteration halo is marked by iron and magnesium enrichment, and calcium and sodium depletion. These features are often only detectable if the over-riding effects of igneous differentiation are compensated. It is apparent that the relative contribution of individual elements to the geochemical alteration varies from deposit to deposit, preventing the recognition of any universal geochemical alteration criterion.The role of discriminant analysis has been examined to establish the possibility of the technique indicating a more reliable expression of geochemical alteration. Discriminant analysis establishes the optimum weighted combination of variables to distinguish two or more populations from each other, in this case mineralized from barren environments. The application of the procedure to the data relating to the composition of wall rock associated with eight volcanic-exhalative massive sulfide deposits has drawn attention to the existence of two distinct types of alteration. The Joutel and Poirier deposits are characterized by Fe₂O₃, MgO, Zn and Ag enrichment, and CaO and Na₂O depletion; this alteration style has been termed the “Joutel” type. At the South Bay, Sturgeon Lake and Mobrun deposits, Na₂O is also strongly depleted, but Fe₂O₃ and MgO are usually depleted and K₂O is strongly enriched; this alteration style has been termed the “South Bay” type. Both of these alteration styles are displayed at the Mattabi and East Waite deposits. “Joutel” type alteration appears to be in close spatial association with discharge vents, while “South Bay” alteration is more laterally widespread and is representative of at least one deposit thought to be formed distally from its associated discharge vent.These geochemical signatures are more strongly expressed in pyroclastic rocks, and andesites, relative to massive rocks, and rhyolites.The geochemical alteration patterns delineated in this way constitute significantly larger exploration targets than the readily observable mineralogical alteration haloes.Results of the current investigations indicate that the mineralizing processes associated with Archean volcanic-exhalative massive sulfide deposits have given rise to more than oversimplification to aim exploration at the detection of a single type of response. The application of discriminant analysis provides a potential means of identifying and comparing as many responses as are present at the deposits studied. In this respect it is superior to any univariate statistical method, and has considerable application in exploration.     

The optical features and hydrocarbon-generating model of “barkinite” from Late Permian coals in South China

Leping coal is known for its high content of “barkinite”, which is a unique liptinite maceral apparently found only in the Late Permian coals of South China. “Barkinite” has previously identified as suberinite, but on the basis of further investigations, most coal petrologists conclude that “barkinite” is not suberinite, but a distinct maceral. The term “barkinite” was introduced by (State Bureau of Technical Supervision of the People's Republic of China, 1991, GB 12937-91 (in Chinese)), but it has not been recognized by ICCP and has not been accepted internationally.In this paper, elemental analyses (EA), pyrolysis-gas chromatography, Rock-Eval pyrolysis and optical techniques were used to study the optical features and the hydrocarbon-generating model of “barkinite”. The results show that “barkinite” with imbricate structure usually occurs in single or multiple layers or in a circular form, and no definite border exists between the cell walls and fillings, but there exist clear aperture among the cells.“Barkinite” is characterized by fluorescing in relatively high rank coals. At low maturity of 0.60–0.80%R_o, “barkinite” shows strong bright orange–yellow fluorescence, and the fluorescent colors of different cells are inhomogeneous in one sample. As vitrinite reflectance increases up to 0.90%R_o, “barkinite” also displays strong yellow or yellow–brown fluorescence; and most of “barkinite” lose fluorescence at the maturity of 1.20–1.30%R_o. However, most of suberinite types lose fluorescence at a vitrinite reflectance of 0.50% Ro, or at the stage of high volatile C bituminous coal. In particular, the cell walls of “barkinite” usually show red color, whereas the cell fillings show yellow color under transmitted light. This character is contrary to suberinite.“Barkinite” is also characterized by late generation of large amounts of liquid oil, which is different from the early generation of large amounts of liquid hydrocarbon. In addition, “barkinite” with high hydrocarbon generation potential, high elemental hydrogen, and low carbon content. The pyrolysis products of “barkinite” are dominated by aliphatic compounds, followed by low molecular-weight aromatic compounds (benzene, toluene, xylene and naphthalene), and a few isoprenoids. The pyrolysis hydrocarbons of “barkinite” are mostly composed of light oil (C₆–C₁₄) and wet gas (C₂–C₅), and that heavy oil (C₁₅⁺) and methane (C₁) are the minor hydrocarbon.In addition, suberinite is defined only as suberinized cell walls—it does not include the cell fillings, and the cell lumens were empty or filled by corpocollinites, which do not show any fluorescence. Whereas, “barkinite” not only includes the cell walls, but also includes the cell fillings, and the cell fillings show bright yellow fluorescence.Since the optical features and the hydrocarbon-generating model of “barkinite” are quite different from suberinite. We suggest that “barkinite” is a new type of maceral.     

Lithological–Facies Features and Formation Conditions of Paleogene Zeolite-Bearing Complexes of the Eastern Ciscaucasus

Paleocene and Eocene terrigenous–siliceous complexes of the Eastern Ciscaucasus contain 18–92% zeolites represented by clinoptilolite. The studied complexes are the stratified subplatformal shallow-water subaqueous deposits with abundant authigenic silica as skeletal remains, cryptocrystalline substance, and pyroclastic material. Clinoptilolite in Paleocene–Eocene terrigenous–siliceous sediments formed from the mud solutions mainly at the expense of the labile pyroclastic material and biogenic silica. Variations in the zeolite abundance are explained by different contents of the pyroclastic material and SiO₂in the primary sediment.     

Mangerite magmatism associated with a probable Late-Permian to Triassic Hongseong–Odesan collision belt in South Korea

The Odesan area in the eastern Gyeonggi Massif, South Korea, consists principally of migmatitic and porphyroblastic gneisses intruded by mangerite. Mafic mangerites with SiO₂ contents from 52.40 to 54.20 wt.% have higher FeO* + MgO (14.98–18.28 wt.%) and CaO contents (5.80–7.84 wt.%) but lower total alkali contents (4.74 < Na₂O + K₂O < 5.80 wt.%) than felsic mangerites (55.9 < SiO₂ < 60.61 wt.%, 9.51< FeO* + MgO < 11.62 wt.%, 3.28 < CaO < 5.68 wt.%, 6.72 < Na₂O + K₂O < 8.05 wt.%). Fe-numbers (FeO* / [MgO + FeO*]) are 0.44–0.47 for mafic mangerites and 0.38–0.42 for felsic mangerites. The mangerites show calc-alkaline affinities in an AFM plot and resemble high-Ba–Sr granitoids with low Rb / Sr ratios of 0.25–0.10. Their MORB-normalized compositions show enrichment in LILE (decoupled LIL/HFS pattern) and negative anomalies in Ti–Nb–Ta. Their geochemical characters are consistent with their formation by partial melting of a basaltic source at temperatures higher than 1025 °C. The mangerites of the present study differ from mangerite formed in a typical within-plate tectonic setting in their high mg# and Sr concentrations and negative Nb and Ta anomalies. Their LILE enrichment and negative Ti–Nb–Ta anomalies could well have been inherited from a pre-collision subduction event. A mean U–Pb zircon age of 257 Ma for the mangerite demonstrates that the tectonic belt connecting the Hongseong and Odesan areas represents a probable extension of the late Permian–Triassic collision belt between the North China and South China blocks into South Korea, with collision occurred earlier in South Korea.     

An investigation of Malaysian granitic rocks as suitable sources of feldspar

Medium- to coarse-grained leucocratic granitic bodies containing more than 60% feldspar and less than 10% mafic minerals are found to be appropriate and potential source materials of local feldspar. Out of the 72 granite quarries/outcrops studied in Peninsular Malaysia, 31 have been identified as “ideal” sources of feldspar conforming to the “preferred” feldspar specification of >18% Al₂O₃, >11% (Na₂O+K₂O) and <0.3% Fe₂O₃. A feldspar recovery efficiency exceeding 60% was achieved in this study. Despite the positive and encouraging indication that the extracted feldspar samples of different chemical composition are found to be suitable for the general purpose of making ceramic bodies and glaze, the chemical content of the feldspar, nevertheless, could be critical for the manufacture of specific end products. At 1250°C all extracted feldspar samples were fused; however, at the lower temperature of 1170°C feldspar samples extracted from some “Central Belt granites” remained unfused. The Eastern Province granites generally yielded feldspars which show better fusion characteristics i.e. (unblemished) than those extracted from the Main Range Province. A valuable by-product of the feldspar extraction process is silica sand.     

Application of lithogeochemistry to exploration for deep VMS deposits in high grade metamorphic rocks, Snow Lake, Manitoba

Volcanic-associated massive sulphide deposits in the Snow Lake area of Manitoba are related to mineralogically and chemically distinct alteration zones. It is generally accepted that these zones represent crosscutting, subconformable or conformable synvolcanic alteration zones, which were coeval with and have been metamorphosed with the massive sulphides. Metamorphism ranges from upper greenschist facies to middle amphibolite facies. Surface lithogeochemical anomalies led to the discovery of small massive sulphide lenses at a vertical depth of 250 m in the Raindrop Lake area, southwest of Snow Lake, Manitoba. Variations in mineral assemblages of middle amphibolite facies alteration zones and analysis of variations in major and trace element chemistry were used to guide deep drilling at Raindrop Lake. The massive sulphide lenses are stratigraphically underlain by a low angle crosscutting “pipe” and a conformable footwall “apron” alteration.The alteration zones are composed of assemblages of garnet, staurolite and chlorite, and, less significantly, biotite, muscovite and kyanite. They are characterized by loss of Na and Ca, and addition of Fe, Mg, Cu and Zn. Mapping the alteration is aided by the application of the metamorphic AFM phase diagram for the appropriate metamorphic facies. Increasing intensity of alteration can be identified by the first appearance of new mineral phases, which are represented on the AFM diagram. These mineral trends coincide with loss of Na and Ca relative to Al, and increased Mg and Fe. Chemical alteration indices ACNK (molecular proportion Al₂O₃/(CaO + Na₂O + K₂O) and AI = 100 × [(MgO + K₂O)/(MgO + K₂O + CaO + Na₂O)] combined with Cu and Zn variation helped to quantify the intensity of alteration, despite being insensitive to Fe.The crosscutting pipe is dominantly Fe enriched, with a Cu-enriched core, Zn enriched margins and widespread Na and Ca depletion. Mineralogically it is identified by garnet, staurolite and chlorite and follows an iron and aluminum enrichment trend on the AFM diagram. The conformable alteration zone is characterized by local strong Mg enrichment, extensive Na and Ca depletion and variable Cu and Zn. Mineralogically it is characterized by the presence of chlorite and kyanite and follows a magnesium and aluminum enrichment trend on the AFM diagram.     

Mineral chemistry and chemical zoning in tourmalines, Pampa del Tamboreo, San Luis, Argentina

Tourmalinites that are distally associated with tungsten deposits of the Pampa del Tamboreo area, San Luis, Argentina, contain tourmalines retaining evidence for its origin and evolution. Tourmaline grains uncommonly contain small grains of detrital tourmaline. Analysis of a single detrital tourmaline grain reveals that it is a Ca-rich “oxy-dravite”. Proximal to the detrital cores there are inner domains of asymmetric tourmaline overgrowths that developed during low grade metamorphism. Volumetrically dominant tourmaline overgrowths in the outer domain are concentrically zoned aluminous dravite and “oxy-dravite” with Al/(Al + Fe + Mg) = 0.71–0.74 and Mg/(Mg + Fe) = 0.64–0.71. Variability of Al is primarily controlled by the deprotonation substitution R + OH⁻ = Al + O²⁻ (where R = Fe + Mg), and is a function of the activity of H₂O. A likely evolutionary scenario is one in which volcanogenic material is altered by hydrothermal fluids in the sea floor resulting in an aluminous and magnesian residuum. With further hydrothermal circulation and incipient metamorphism, boron-rich fluids are expelled from metasedimentary and metavolcanic basement rocks and develop Mg-rich tourmalinites in the aluminous, magnesian host rocks. The tourmalinization process occurs over a range of metamorphic conditions and with fluids of variable activity of H₂O.     

Solid inclusions of magmatic halite and sylvite in felsic granitoids, Sierra Norte, Córdoba, Argentina

This study provides evidence for the existence of halite and sylvite solid inclusions in igneous quartz and feldspars, the first to be reported in intrusive rocks, and to partially constrain the physicochemical environment that lets halides crystallize under magmatic conditions.Halite and sylvite solid inclusions were found included in quartz and feldspars from a micrographic–granophyric assemblage in a miarolitic aplite and, rarer, in alkali-feldspar from a miarolitic monzogranite. Monzogranite and aplite represent I-type, K-enriched postcollisional rocks of the Late Cambrian–Early Ordovician Sierra Norte–Ambargasta batholith in the Eastern Sierras Pampeanas. Both granitoids fall among the most evolved felsic rocks of the batholith, with aplite approaching haplogranitic compositions. Halite is far more common than sylvite and the presence and distribution of one or both halides are erratic within the felsic intrusive bodies. Halides occur as small skeletal grains, commonly in cross-shaped aggregates of less than 50 μm. No K or Na was found at the detection limits of EDS in either halite or sylvite respectively. Textural relationships suggest that the alkali-chlorides separated from the melt near the minima along the quartz–feldspar cotectics of P_H2O > 160 < 200 MPa in a silica-, and potassium-rich magmatic system at approximately 750–700 °C, prior to the H₂O-vapor saturated miarole-forming stage.Computed ratios for the magmatic volatile phase (MVP) coexisting with melt at the early stage of aplite crystallization are: NaCl/HCl = 0.11–0.97 and KCl/HCl = 0.24–1.62, being the highest range of values (0.79–0.97 and 1.45–1.62, respectively) found in those alkali-chloride-bearing samples. Maximum HCl/ΣCl_(MVP) (0.28 to 0.31) indicates higher total Cl concentration in the MVP of alkali-chloride-bearing aplites, which is much higher in the halite-free aplite samples (HCl/ΣCl_(MVP) = 0.59 to 0.74). One miarolitic monzogranite sample, where halite solid inclusions are present, also yielded the highest ratios for NaCl/HCl_(MVP) (0.91) and KCl/HCl_(MVP) (1.46), and the HCl/ΣCl_(MVP) is 0.30. A high HCl concentration in the fluid phase is suggested by the log f(HF)/f(H₂O) = − 4.75 to − 4.95, log f(HCl)/f(H₂O) = − 3.73 to − 3.86, and log f(HF)/f(HCl) = − 0.88 to − 1.22, computed at 750 °C after biotite composition. The Cl concentrations at 800 °C, computed with a D^v/l_Cl = 0.84 + 26.6P (P at 200 MPa), yielded values within the range of  70 to 700 ppm Cl in the melt and  4000 to 40 000 ppm Cl in the coexisting MVP. The preferential partitioning of Cl in the vapor phase is controlled by the D^v/l_Cl; however, the low concentration of Cl in the melt suggests that high concentrations of Cl are not necessary to saturate the melt in NaCl or KCl.Cl-saturation of the melt and coexisting MVP might have been produced by a drop in Cl solubility due to the near-haplogranitic composition of the granitoids after extreme fractionation, probably enhanced by fluctuating reductions of the emplacement pressure in the brittle monzogranite host. Liquid immiscibility, based in the differential viscosity and density among alkali-chloride saturated hydrosaline melt, aluminosilicate felsic melt, and H₂O-rich volatiles is likely to have crystallized halite and sylvite from exsolved hydrosaline melt. High degrees of undercooling might have been important at the time of alkali-chloride exsolution. The effectiveness of alkali-chloride separation from the melt at magmatic temperatures is in line with the interpretation of “halite subtraction” as a necessary process to understand the origin of the “halite trend” in highly saline fluid inclusions from porphyry copper and other hydrothermal mineralizations, despite the absence of the latter in the Cerro Baritina aplites, where this process preceded the exsolution of halite-undersaturated fluids.Pervasive alteration of the monzogranite country rock as alkali-metasomatic mineral assemblages, the mineral chemistry of some species, and the association of weak molybdenite mineralization are compatible with the activity of alkaline hypersaline fluids, most likely exsolved during the earliest stages of aplite consolidation.     

Tectonomagmatism in continental arcs: evidence from the Sark arc complex

The island of Sark (Channel Islands, UK) exposes syntectonic plutons and country rock gneisses within a Precambrian (Cadomian) continental arc. This Sark arc complex records sequential pulses of magmatism over a period of 7 Ma (ca. 616–609 Ma). The earliest intrusion (ca. 616 Ma) was a composite sill that shows an ultramafic base overlain by a magma-mingled net vein complex subsequently deformed at near-solidus temperatures into the amphibolitic and tonalitic Tintageu banded gneisses. The deformation was synchronous with D₂ deformation of the paragneissic envelope, with both intrusion and country rock showing flat, top-to-the-south LS fabrics. Later plutonism injected three homogeneous quartz diorite–granodiorite sheets: the Creux–Moulin pluton (150–250 m; ca. 614 Ma), the Little Sark pluton (>700 m; 611 Ma), and the Northern pluton (>500 m; 609 Ma). Similar but thinner sheets in the south (Derrible–Hogsback–Dixcart) and west (Port es Saies–Brecqhou) are interpreted as offshoots from the Creux–Moulin pluton and Little Sark pluton, respectively. All these plutons show the same LS fabric seen in the older gneisses, with rare magmatic fabrics and common solid state fabrics recording syntectonic crystallisation and cooling. The cooling rate increased rapidly with decreasing crystallisation age: >9 Ma for the oldest intrusion to cool to lower amphibolite conditions, 7–8 Ma for the Creux Moulin pluton, 5–6 Ma for the Little Sark pluton, and <3 Ma for the Northern pluton. This cooling pattern is interpreted as recording extensional exhumation during D₂. The initiation of the D₂ event is suggested to have been a response to the intrusion of the Tintageu magma which promoted a rapid increase in strain rate (>10⁻¹⁴ s⁻¹) that focussed extensional deformation into the Sark area. The increased rates of extension allowed ingress of the subsequent quartz diorite–granodiorite sheets, although strain rate slowly declined as the whole complex cooled during exhumation. The regional architecture of syntectonic Cadomian arc complexes includes flat-lying “Sark-type” and steep “Guernsey-type” domains produced synchronously in shear zone networks induced by oblique subduction: a pattern seen in other continental arcs such as that running from Alaska to California.