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The Hera Au–Pb–Zn–Ag deposit in the southeastern Cobar Basin of central New South Wales preserves calc-silicate veins and remnant sandstone/carbonate-hosted skarn within a reduced anchizonal Siluro-Devonian turbidite sequence. The skarn orebody distribution is controlled by a long-lived, basin margin fault system, that has intersected a sedimentary horizon dominated by siliciclastic turbidite, with lesser gritstone and thick sandstone intervals, and rare carbonate-bearing stratigraphy. Foliation (S1) envelopes the orebody and is crosscut by a series of late-stage east–west and north–south trending faults. Skarn at Hera displays mineralogical zonation along strike, from southern spessartine–grossular–biotite–actinolite-rich associations, to central diopside-rich–zoisite–actinolite/tremolite–grossular-bearing associations, through to the northern most tremolite–anorthite-rich (garnet-absent) association in remnant carbonate-bearing lithologies and sandstone horizons; the northern lodes also display zonation down dip to garnet present associations. High-T, prograde skarn assemblages rich in pyroxene and garnet are pervasively replaced by actinolite/tremolite–biotite-rich retrograde skarn which coincides with the main pulse of sulfide mineralization. The dominant sulfides are high-Fe–Mn sphalerite–galena–non-magnetic high-Fe pyrrhotite–chalcopyrite; pyrite, arsenopyrite; scheelite (low Mo) is locally abundant. The distribution of metals in part mimics the changing gangue mineralogy, with Au concentrated in the southern and lower northern lode systems and broadly inverse concentrations for Ag–Pb–Zn. Stable isotope data (O–H–S) from skarn amphiboles and associated sulfides are consistent with magmatic (or metamorphic) water and sulfur input during the retrograde skarn phase, while hydrosilicates and sulfides from the wall rocks display comparatively elevated δD and mixed δ34S consistent with progressive mixing or dilution of original magmatic (or metamorphic) waters within the Hera deposit by unexchanged waters typical of low latitude (tropical) meteoritic waters. High precision titanite (U–Pb) and biotite (Ar–Ar) geochronology reveals a manifold orebody commencing with high-T skarn and retrograde Pb–Zn-rich skarn formation at ≥403 Ma, Au–low-Fe sphalerite mineralization at 403.4 ± 1.1 Ma, foliation development remobilization or new mineralization at 390 ± 0.2 Ma followed by thrusting, orebody dismemberment at 384.8 ± 1.1 Ma and remobilization or new mineralization at 381.0 ± 2.2 Ma. The polymetallic nature of the Hera orebody is a result of multiple mineralization events during extension and compression and involving both magmatic and likely formational metal sources.

Rocks of gabbronoritic composition occur in three principal tectono-stratigraphic units forming the lower and middle parts of the Kohistan Island arc (KIA). These include the Jijal complex (JC), the Kamila Amphibolite belt (KAB) and the Chilas complex (CHC). The Jijal complex constitutes the lowermost part and hence is regarded as the root zone of KIA. Its north-eastern part adjacentto KAB contains gabbronorite as a minor component in the form of small irregular patches and layers within garnet granulite. The JC gabbronorite is sub-equigranular, medium to coarse grained, largely massive and consists of variable amounts of plagioclase(53-71 %), orthopyroxene (14-27 %) and clinopyroxene (11-19 %) as essential constituents and accessory to minor amounts of amphibole (1-9 %), opaque ore (1-6 %) and orthoclase (1-4 %). The occurrence and distribution of biotite, epidote, chlorite, clay, sericite, muscovite, quartz and actinolite in the studied samples suggest their formation through alteration and/ or reaction between pre-existing minerals. In many cases, these minerals are disposed such that a variety of simple and complex corona structures are produced. The principal petrographic features (modal composition, optical properties of the major mineral phases, exsolution in pyroxenes, products of alteration and reactions and the resulting corona textures) of the JC gabbronorite are broadly similar to gabbronorites from both the KAB and CHC. Although the observed similarities could reflect identical physico-chemical conditions during subsolidus or metamorphic re-equilibration, the possibility of a genetic relationship among gabbronorites from all the three tectono-magmatic units of the KIA (i.e. the JC, KAB and CHC) cannot be ruled out.

Background/Objectives: Talcose rocks within Precambrian Basement Complex serve as relics of Archean greenstones. alterations associated with polycyclic-orogenies that affected this complex is studied to understand mineralogical and geochemical alterations. Methods: Five fresh samples of talcose rocks were collected during field mapping. These samples were cut into thin sections to reveal modal mineralogy, altered minerals and degree of alteration of such minerals. Mineral phase identification of the talcose rocks was conducted using X-ray Broker D8 ADVANCE diffractometer while whole rock analysis was carried out using Inductively Coupled Plasma Mass Spectrometry. Findings: Lithological relationship revealed from field evidence showed that the talc bodies occurred in close association with micaceous schist. The mineral assemblage of talc, tremolite, actinolite, chlorite and calcite suggest low grade greenschist metamorphic facies from possible hydrothermal alteration. Geochemical results revealed the following range of concentrations; SiO2 42.19-59.03%; Al2O3 1.1 - 11.8%; Fe2O3 7.64-9.56%; MgO 24.47-26.639%; Ni 594-1207ppm; Co 43.2-113.9ppm; Sn 6-41ppm; V 32-75ppm and Zr 1.3-58.7ppm, and these are typical of talcose rocks. Petrogenetic studies suggest a komatiitic origin with a peridotitic komatiite precursor for the talc-chlorite-tremolite schist. Enrichment in LREE, depletion in HREE and a negative Eu anomaly suggest alteration of the parent magma for the talcose rock and plagioclase fractionation. The trends observed for the LILE, HFSE and REE suggest possible contamination or mixing of crustal and mantle materials during the formation of the protolith. Ni and Co concentrations are higher than average crustal values with implication for ultrabasic to basic magma composition for the komatiitic progenitor and also suggestive of possible mineralisation. Conclusion: Mineralogical examination has revealed a talc-chlorite-tremolite composition for the talcose rocks with peridotitic komatiite precursory while geochemical composition supported ultrabasic magmatism similar to those with the Ilesha schist belt.Keywords: Ila Orangun-Oyan; Talcose rocks; Hydrothermal alteration; Peridotitic Komatiite; Ilesha schist belt

As rochas ortoderivadas de composição básicas e ultrabásicas são constituídas por anfibolitos, metabasitos e metaultrabásitos de idade meso- a neoproterozoica, que se localizam no sudoeste do estado de São Paulo, na porção sul do Cinturão Ribeira e norte do Terreno Apiaí. Encontram-se inseridas em rochas da sequência metavulcanossedimentares do Supergrupo Açungui, especificamente na Formação Água Clara e no Grupo Itaiacoca. A paragênese mineral principal é constituída de ferrotschermakita- ferrohornblenda- magnesiohornblenda ± oligoclásio/andesina, representando o ápice do metamorfismo regional progressivo M1, de 611°C a 621°C de temperatura e 6,5 kbar a 7,3 kbar (±0,6) (Fácies anfibolito médio); e uma paragênese mineral de actinolita/tremolita ± albita, do retrometamorfismo regional M3 (fácies xisto verde baixo a médio). Dados geoquímicos composicionais classificam as rochas como gabro, basanito e picrito, sub alcalinos de baixo potássio a alcalinos, Fe-toleíticos a Mg-toleíticos, com leve tendência à basaltos komatiíticos. Já os dados geotectônicos, corroborados pelo comportamento dos elementos traços e dos ETRs, indicam três assinaturas principais para os grupos anfibolíticos: rochas básicas toleíticas a komatiíticas associadas a cadeia mesoceânicas (MORB), com possível interação da crosta na fase de subducção; rochas ultrabásicas alcalinas de ilha oceânica (OIA); e basaltos toleíticos de arco de ilha. Portanto, os magmatismos estão correlacionados ao estágio inicial de abertura de bacia ou ao início de fechamento à fase inicial de natureza toleítica de fundo oceânico, associado a basaltos alcalinos de ilha oceânica.

The onset of malignant mesothelioma (MM) is linked to exposure to asbestos fibers. Asbestos fibers are classified as serpentine (chrysotile) or amphibole, which includes the crocidolite, amosite, anthophyllite, tremolite, and actinolite types. Although few studies have been undertaken, anthophyllite has been shown to be associated with mesothelioma, and tremolite, a contaminant in talc and chrysotile, is a risk factor for carcinogenicity. Here, after characterizing the length and width of these fibers by scanning electron microscopy, we explored the cytotoxicity induced by tremolite and anthophyllite in cells from an immortalized human mesothelial cell line (MeT5A), murine macrophages (RAW264.7), and in a rat model. Tremolite and short anthophyllite fibers were phagocytosed and localized to vacuoles, whereas the long anthophyllite fibers were caught on the pseudopod of the MeT5A and Raw 264.7 cells, according to transmission electron microscopy. The results from a 2‐day time‐lapse study revealed that tremolite was engulfed and damaged the MeT5A and RAW264.7 cells, but anthophyllite was not cytotoxic to these cells. Intraperitoneal injection of tremolite in rats induced diffuse serosal thickening, whereas anthophyllite formed focal fibrosis and granulomas on peritoneal serosal surfaces. Furthermore, the loss of Cdkn2a/2b, which are the most frequently lost foci in human MM, were observed in 8 cases of rat MM (homozygous deletion [5/8] and loss of heterozygosity [3/8]) by array‐based comparative genomic hybridization techniques. These results indicate that tremolite initiates mesothelial injury and persistently frustrates phagocytes, causing subsequent peritoneal fibrosis and MM. The possible mechanisms of carcinogenicity based on fiber diameter/length are discussed., MeT5A (immortalized mesothelial cells) and RAW264.7 (macrophage lineage cells) were damaged by tremolite but not anthophyllite. Tremolite induced diffuse peritoneal thickening, whereas anthophyllite induced focal fibrosis. Furthermore, tremolite‐induced malignant mesothelioma frequently lost Cdkn2a/2b.

Heavy mineral assemblages have been widely used to effectively trace sediment sources. Heavy mineral assemblages are rarely used in research to trace sediment sources in the southern Okinawa Trough compared with geochemical proxies. In this study, the TESCAN Integrated Mineral Analyzer (TIMA) revealed the full-size heavy mineral assemblages in the five layers of the core sediment H4-S2 in the southern Okinawa Trough. During the past 700 years, the heavy mineral assemblages in the sediments of the southern Okinawa Trough were very similar to the East China Sea shelf/Yangtze River, mainly composed of mica and chlorite, dolomite, actinolite, and hematite/magnetite. The grain size distribution of heavy minerals is in the clay–sand range and mainly in silt. Actinolite and hornblende can indicate the supply of sediments from the East China Sea shelf/Yangtze River to the southern Okinawa Trough. Due to their complex sources, pyrite, epidote, and hematite/magnetite are not adequate indicators for distinguishing between the different provenance areas. Because previous studies have used a variety of analytical methods, especially using heavy liquids with different densities, dolomite cannot be used as a marker for sediments on the Yangtze River/East China Sea shelf. Therefore, the East China Sea shelf/Yangtze River is a vital provenance of sediments from the southern Okinawa Trough since the late Holocene period.

This study determines the properties of hot spring waters and associated rocks, calculates reservoir temperatures and depths in the Mongolian Altai region, and constructs a conceptual model for geothermal water based on these results. The hot springs consist of HCO3-Na, SO4-Na, and HCO3-SO4-Na mixed type waters. The waters exhibit alkaline pH levels and temperatures in the range of 21.3–35°C. X-ray diffraction analyses of outcrop rocks reveal silicate and carbonate-type minerals such as quartz, albite, orthoclase, dolomite, mica, and actinolite, while correlation analysis indicates that the chemical composition of the hot spring water is directly related to rock mineral composition. Dissolution of albite, orthoclase, and dolomite minerals has played an important role in the chemical composition of the waters. Reservoir water circulation depths were 2615–3410 m according to quartz and chalcedony geothermometry. The results indicate that the spring water in the Mongolian Altai region comprises a low mineral content with alkaline pH levels and the reservoir temperature can reach up to 106°C. We also propose a conceptual model for geothermal water in the Chikhertei hot spring. The geothermal water in the Mongolian Altai region exhibits a potential for use in heating systems. Thematic collection: This article is part of the Hydrochemistry related to exploration and environmental issues collection available at: https://www.lyellcollection.org/cc/hydrochemistry-related-to-exploration-and-environmental-issues

Iron oxide-copper-gold deposits are a globally important source of copper, gold and critical commodities. However, they possess a range of characteristics related to a variety of tectono-magmatic settings that make development of a general genetic model challenging. Here we investigate micro-textural and compositional variations in actinolite, to constrain the thermal evolution of the Candelaria iron oxide-copper-gold deposit in Chile. We identify at least two mineralization stages comprising an early 675–800 °C iron oxide-apatite type mineralization overprinted by a later copper-rich fluid at around 550–700 °C. We propose that these distinct stages were caused by episodic pulses of injection of magmatic-hydrothermal fluids from crystallizing magmas at depth. We suggest that the mineralisation stages we identify were the result of temperature gradients attributable to changes in the magmatic source, rather than variations in formation depth, and that actinolite chemistry can be used as a proxy for formation temperature in iron oxide-copper-gold systems. The Candelaria iron oxide-copper-gold deposit in Chile was formed by superimposed, episodic hydrothermal pulses with contrasting composition and temperature, according to micro-textural and compositional variations in actinolite, a common alteration mineral.

This study presents petrology and evidence for possible gold occurrences in Seruwila copper–iron oxide–apatite (IOA) deposit, hosted in an ultramafic intrusion which is located at the boundary between the Highland and Vijayan complexes, within the intermediate-granitic basement in north-eastern Sri Lanka. The study is complemented with petrological observations and XRD and SEM analysis, respectively, to investigate the petrology/subsurface geology of the deposit and identify possible gold occurrences in the deposit. The ore-bearing rocks are mainly composed of magnetite and apatite in various proportions, hosted in an ultramafic intrusion with cumulate features within the granitic-intermediate basement. The secondary veins contain magnetite, chalcopyrite, pyrrhotite, and pyrite together with apatite and scapolite, tremolite, diopside, and minor actinolite and calcite, serpentinite, anhydrite, or gypsum. The clinopyroxene euhedral crystals show cumulus textures including grain triple junctions and large dihedral angles (∼120°), showing magmatic origin. Texturally two types of amphiboles are identified as coarse-grained (0.5–1 mm), pale green euhedral amphibole that is free of inclusions, and fine-grained (

Nielsenite, a rare intermetallide of palladium and copper, was described previously as a late-magmatic formation. A different genetic type of nielsenite was studied in the layered ultrabasite–basite Yoko-Dovyren intrusive. The maximum concentrations of Pd, Pt, Au, and Ag minerals are confined to crosscutting bodies of pegmatoid sulfide-bearing anorthosites within the contact zone between the troctolites and overlapping gabbro-norites strata in this intrusive. Postmagmatic pneumatolytic (fluid-metasomatic) Pd, Pt, Au, and Ag minerals, such as kotulskite, moncheite, michenerite, zvyagintsevite, telargpalite, paolovite, electrum, and sperrillite, compose metasomes in Fe–Ni–Cu sulfides and in the silicate matrix nearby. The Yoko-Dovyren intrusive is tectonized and tilted, crossed by inclined faults with streamlined serpentinized rocks, which contain lizardite, antigorite, clinozoisite, chlorite, actinolite, prehnite, pectolite, and hydrogarnet and are often transformed into rodingites of a prehnite–pumpellyite facies. The serpentinization process is younger than the intrusive rocks by 55 million years. In metamorphosed anorthosites, chalcopyrite is replaced by bornite, chalcocite, digenite, and magnetite; pentlandite is replaced with violarite, heazlewoodite, …; pyrrhotine is replaced by magnetite, …; moncheite is replaced with cuproplatinum–tulameenite; the veins of clinozoisite and pectolite with chlorite inclusions of chalcosine and native copper are well developed. Curved veins of nielsenite in brecciated chalcopyrite occasionally extend such veins. The size of the veins of metamorphogenic-hydrothermal nielsenite reaches up to 200 × 10 microns. Nielsenite metasomes up to 12 microns in diameter are developed nearby. The composition of the Yoko-Dovyren nielsenite is stable and close to stoichiometric with the formula Pd1.01Cu2,81Fe0,17Ni0,01. The Yoko-Dovyren nielsenite differs from the holotype of nielsenite of the Skergaard intrusive by the absence of Pt and Au impurities and a significant impurity of Fe. Yoko-Dovyren nielsenite was likely to appear under conditions of the prehnite–pumpellyite metamorphism facies at a high fugacity of О2 and at an extremely low fugacity of sulfide sulfur (log f S2 < –24 at ≈300°C).

International audience; Asbestos consists in natural minerals crystallized in a specific habit and possessing in particular properties. In the case of Naturally Occurring Asbestos, usual methods applied to the identification of mineral fibers and the determination of their possible asbestiform nature seems not efficient, especially in the case of mineral fibers included in mineral matrix. We present a new in-situ method based on the use of confocal Raman-in-SEM imaging implemented in a Scanning Electron Microscope as an efficient method for in-situ mineralogy. The limitation of conventional methods is discussed. We applied 2D-Raman imaging to the identification of sub-micrometric fibers included in different mineral matrix. We were able to identify actinolite fibers down to 400 nm in diameter, included in feldspar, quartz and/or calcite matrix. Moreover, Confocal Raman allows the collection of 3D data that would provide access to critical information on the morphology of the amphibole fibers in the volume, such as aspect ratio, fibers distribution and amphibole volume fraction. We performed this method on various examples of rocks containing actinolite fibers of mean structural formula is: Na0,04-0,12Mg2,79-3,73Al0,29-0,58K0,01Ca1,79-1,98Mn0,01-0,09Fe 2+ 0,99-1,91Fe 3+ 0,12-0,25Si7,64-7,73O22(OH)2. We demonstrated that coupling confocal Raman imaging and SEM is a new and efficient in-situ method for identification and morphological characterization of amphibole fibers. Highlights New methods are requested for characterizing asbestos fibers in a mineral matrix SEM-Raman imaging is efficient for characterizing mineral fibers in-situ Confocal Raman imaging makes 3D analysis possible 3D analysis provides information on the aspect ratio and volume fraction of asbestos Fibers thinner than 400nm can be identified by confocal Raman in SEM ( = 532 nm)

Actinolite is one of the six minerals belonging to the group of asbestos minerals. There is increasing concern regarding the potential health risks from exposure to naturally occurring asbestos and asbestos-containing materials. The correct distinction of the fibrous asbestos minerals is very important not only from a scientific point of view, but also from a legislative perspective. Asbestos actinolite is currently the only asbestos mineral that has not been fully characterized from the thermal point of view. In order to compensate for this gap in scientific literature, this paper discusses the thermal behaviour of actinolite asbestos using thermogravimetric and differential scanning calorimetry. X-ray powder diffraction, Scanning and Transmission Electron Microscopy combined with energy-dispersive spectrometry were used for the characterization of actinolite fibres before and after heating at 1000 and 1200 °C in order to determine their resistance to high-temperature changes and the products of thermal recrystallization. Actinolite asbestos breaks down at approximately 1030 °C. The thermal decomposition process of actinolite asbestos consists of two distinct events followed by recrystallization into new stable crystalline phases which preserved the original fibrous morphology (known as pseudomorphosis). The thermal analysis may prove to be useful for actinolite identification and discrimination, particularly in the case of natural massive samples where asbestos tremolite–actinolite amphiboles are mutually intermixed. Furthermore, profound knowledge of the thermal behaviour of this asbestos mineral may provide us with the relevant data for understanding the crystal–chemical transformations of asbestos through thermal inertization treatment.

Research subject . High-magnesium rocks associated with the granitoid massifs of the Urals are represented by gabbro-diorites and their melanocratic varieties (hornblendites), as well as by diorites and quartz diorites. These rocks are composed of amphibole porphyrocrists frequently combined with clinopyroxene and phlogopite immersed in a basis of acid plagioclase with interstitial quartz and potassium feldspar. In addition to a high magnesium content of 0.5–0.8 units, these rocks are characterized by extremely high chromium contents of up to 1200 ppm. Methods . The study of the composition of high-magnesium rocks was performed using an ELAN 9000 inductively coupled plasma mass spectrometer, an SX-100 Cameca electron probe microanalyzer and an energy dispersive device INCAEnergy 450 X-Max 80. The detection limit for Cr 2 O 3 was equal to 0.05 wt. % and 0.2 wt. % for the microanalyzer and the energy dispersive device, respectively. Results . The two main mineral associations related to magmatic and post-magmatic processes are found to be different in terms of chromium behaviour. The average concentrations of chromium oxide in the minerals from the magmatic association varied within the range (wt. %) of 0.10–0.50, 0.29–0.68, 0.08-0.36 and 0.0–1.6 for different samples of clinopyroxene, amphibole, phlogopite and their variations, respectively. The post-magnetic association included minerals representing the products of postmagmatic (hydrothermal) transformation of pyroxenes and alumina amphibole into low-alumina magnesia hornblende, actinolite, titanite, epidote and muscovite. The transformation of chromospinelide at this stage had been accompanied by exchange processes with silicates, as a result of which the silicates were enriched with chromium. The average concentrations of chromium oxide in the minerals of this association were (wt. %) 0.24–0.80, 1.38–3.08, 1.03 and 3.5 in the samples of amphibole, epidote, titanite and muscovite, respectively. Conclusion . It is assumed that the crystallization of the early association of iron-magnesium silicates proceeded from aqueous high-magnesium melts. The subsequent post-magmatic change of such silicates led to the development of phases with a similar and occasionally higher chromium content. This fact can be explained by the interaction of silicates with chromite under the conditions of low fluid oxidation, which was insufficient for the formation of magnetite.

The Arqiale deposit, located in the southern Yili Block of Western Tianshan, Xinjiang, China, is a newly discovered large Zn-Pb deposit with a resource of approximately 10 million tons ore grading 9.65% Zn+Pb, and a certain amount of Cu and Ag. The Zn-Pb orebodies are tabular and lentoid in shape, developed along SW-striking and NW-dipping interlayer structures between the Lower Carboniferous Akeshake (mainly carbonate rocks) and Dahalajunshan (mainly volcanic rocks) formations. Garnet and pyroxene-rich skarn, formed in the early (prograde) stage of skarnization, occurs only locally as lenses within skarn bodies enriched in actinolite, tremolite, ilvaite, biotite, epidote, chlorite, calcite, quartz and fluorite, which were formed in the retrograde stage. Metallic minerals comprise sphalerite, galena, chalcopyrite, pyrite, and hematite. They mainly occur as disseminations, patches and massive ores, replacing retrograde skarn minerals and crosscut by later stage quartz and calcite veinlets. There is a general trend of increasing Cu contents and decreasing Zn/Pb ratios from the upper and south portion to the lower and north portion of the orebody. Rb-Sr dating of seven sphalerite samples yielded an isochron age of 339.5 ± 2.7 Ma, which is almost identical to the 341.8 ± 2.5 Ma age obtained from Sm-Nd dating of eight actinolite samples. Furthermore, zircon U-Pb dating yielded an age of 343 ± 6 Ma for a gabbro-diorite stock that is located about 600 m south of the Zn-Pb orebody. The age data indicate that the mineralization and retrograde skarnization were contemporaneous, and they are likely related to a magmatic intrusion of similar age which may be linked to the gabbro-diorite stock. Thus, although the direct causative intrusion has not been identified, the Arqiale deposit can be classified as a distal skarn deposit. The δ34SV-CDT values of 26 ore sulfide samples range from −7.1‰ to +1.3‰ with an average of −1.5‰. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of 25 ore sulfide samples range from 18.266 to 18.880, 15.577 to 15.668 and 38.068 to 38.720, respectively, which are similar to the Early Carboniferous intrusions of the Wusun Range and partly overlap with the volcanic rocks of the Dahalajunshan Formation, and are different from the carbonate rocks of the Akeshake Formation. Based on these data, we propose that the Arqiale deposit formed from magmatic-hydrothermal fluids emanated from a concealed magmatic intrusion which may be located beneath the northern and deep part of the deposit. Much of the metals and sulfur may have been derived from the magmatic intrusions, although some of them may have also been extracted from the volcanic rocks underlying the deposit. The results of this study indicate that there is a great potential of finding more skarn Zn-Pb mineralization in Western Tianshan, where numerous Early Carboniferous arc-related intrusions with similar ages as the Arqiale deposit, in relation to the subduction of the Southern Tianshan Oceanic plate underneath the Yili-Central Tianshan Block, were emplaced into or beneath carbonate rocks.

Hydrous phases have been identified to be a significant component of martian mineralogy. Particularly prehnite, zeolites, and serpentine are evidence for low‐grade metamorphic reactions at elevated temperatures in mafic and ultramafic protoliths. Their presence suggests that at least part of the martian crust is sufficiently hydrated for low‐grade metamorphic reactions to occur. A detailed analysis of changes in mineralogy with variations in fluid content and composition along possible martian geotherms can contribute to determine the conditions required for subsurface hydrous alteration, fluid availability and rock properties in the martian crust. In this study, we use phase equilibria models to explore low‐grade metamorphic reactions covering a pressure‐temperature range of 0‐0.5 GPa and 150‐450 °C for several martian protolith compositions and varying fluid content. Our models replicate the detected low‐grade metamorphic/hydrothermal mineral phases like prehnite, chlorite, analcime, unspecified zeolites, and serpentine. Our results also suggest that actinolite should be a part of lower‐grade metamorphic assemblages, but actinolite may not be detected in reflectance spectra for several reasons. By gradually increasing the water content in the modeled whole rock composition, we can estimate the amount of water required to precipitate low‐grade metamorphic phases. Mineralogical constraints do not necessarily require an elevated geothermal gradient for the formation of prehnite. However, restricted crater excavation depths even for large impact craters are not likely sampling prehnite along colder gradients, either suggesting a geotherm of ~ 20 °C/km in the Noachian or an additional heat source such as hydrothermal or magmatic activity.

The Jalal-Abad iron oxide ± Cu ± Au ± Bi ± Co deposit is hosted in Early Cambrian volcanosedimentary units (CVSU) of the Kashmar–Kerman zone, Central Iran. Magnetite is the main ore mineral at depth and is associated with Na-Ca rich alteration, dominated by actinolite. Magnetite compositions (EPMA) are very low in TiO2 (0.03–0.07 wt%), V2O3 (0.02–0.06 wt%) and CoO (0.01> to 0.42 wt%). At intermediate to shallow levels potassic alteration is associated with chalcopyrite, pyrite, arsenopyrite, cobaltite, bismuthinite and gold. The mineralization occurs in massive, breccia matrix, open space filling, disseminated and vein-like styles. Gold occurs as small inclusions (

The Taochong iron deposit is one of the important skarn deposits in the Middle–Lower Yangtze River metallogenic belt, Eastern China. There are two types of ores in the deposit: skarn- and quartz–calcite-type ores. The skarn-type ore, which is composed of hematite (Hm-1), garnet, pyroxene, actinolite, chlorite, quartz (Q-1), and calcite (Cal-1), is crosscut locally by a quartz–calcite-type ore vein. The quartz–calcite-type ore consists mainly of hematite (Hm-2), magnetite, quartz (Q-2 and 3), and calcite (Cal-2). The δ18Owater value (~2.67‰) of the fluids in equilibrium with Hm-1 is similar to the values of the mixtures of magmatic and meteoric fluids. However, the δ18O values of the fluids in equilibrium with Hm-2 are in the range of 7.64–8.54‰, similar to those of magmatic fluids. The δ18O values decrease systematically from the fluids in equilibrium with Hm-2 (7.64‰ to 8.54‰) to the fluids in equilibrium with magnetite, Q-3, and Cal-2 (−0.12‰ to 4.17‰) and the fluids in equilibrium with Cal-3 (−2.17‰ to 0.36‰). These features of oxygen isotopes indicate that two episodes of hydrothermal activity took place in the Taochong deposit, and both episodes began with a magmatic origin and then progressively evolved by mixing with meteoric water. The results of quantitative simulations suggest that the deposition of the skarn-type ores was most likely caused by the mixing of magmatic and meteoric fluids, whilst the deposition of the quartz–calcite-type ores was most likely caused by the boiling of magmatic fluids and the mixtures of magmatic brine and meteoric water.

The Paraná emerald deposit is one of the few occurrences of emerald, a rare beryl variety, in Borborema Province, northeastern Brazil. We characterized the Paraná deposit by combining field geology, petrography, whole-rock geochemistry, mineral chemistry, and reflectance spectroscopy. The mineralization is associated with phlogopite-, actinolite-phlogopite-, and phlogopite-phengite schists, mylonitic gneisses, and several acidic rocks (e.g. granitic pegmatites/aplites, quartz ± feldspar veins) along the Portalegre Shear Zone. Emerald can be found in quartz-feldspar and aplite veins and veinlets interleaved with phlogopite- or actinolite-phlogopite schists, or within the foliation of the schists. The presence of albitites and the compositional variation of the schists suggest a metasomatic origin for emerald with variations of the metasomatic process. All these different lithotypes can be readily identified through reflectance spectroscopy especially in the range of 2,150-2,450 nm, where the main mafic minerals show absorption features related to Al-OH (phengite), and Fe-OH and Mg-OH bonds (phlogopite/actinolite). Our study shows that possible mineralized phlogopite schists can be distinguished from other sterile rocks, although point spectral analysis does not separate emerald-bearing phlogopite schists from schists without emerald due to the dominance of major phlogopite absorption features rather than emerald features.

The term asbestos refers to a group of serpentine (chrysotile) and amphibole (amosite, crocidolite, anthophyllite, tremolite and actinolite) minerals with a fibrous habit. Their chemical-physical properties make them one of the most important inorganic materials for industrial purposes and technological applications. However, the extraction, use and marketing of these minerals have been prohibited due to proven harmful effects, mainly involving the respiratory system. In addition to the known six minerals classified as asbestos, the natural amphiboles and serpentine polymorphs antigorite and lizardite, despite having the same composition of asbestos, do not have the same morphology. These minerals develop chemical and geometric (length > 5 μm, width < 3 μm and length: diameter > 3:1), but not morphological, analogies with asbestos, which is regulated by the WHO. The debate about their potential hazardous properties is open and ongoing; therefore, their morphological characterization has a key role in establishing a reliable asbestos hazard scenario. This review focuses on evaluating the most relevant papers, evidencing the need for a reappraisal. Different in vitro, in vivo and epidemiological studies report information about cleavage fragments with critical dimensions similar to asbestos fibres, but very few works target fragments below 5 µm in length. Breathable smaller fibres could have deleterious effects on human health and cannot be disregarded from the risk assessment process. Furthermore, a few studies suggest that the carcinogenic nature of short fibres is not excluded. This review highlights that it is worth investigating the effects of this size range of elongated mineral particles and fibres.

Malignant mesothelioma is an aggressive cancer associated with exposure to asbestos. Diagnosis of mesothelioma and other related lung diseases remains elusive due to difficulties surrounding identification and quantification of asbestos fibres in lung tissue. This article presents a laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) method to identify asbestos fibres in cellular models of mesothelioma. Use of a high-speed laser ablation system enabled rapid imaging of the samples with a lateral resolution of 3 μm, whilst use of a prototype time-of-flight ICP-MS provided pseudo-simultaneous detection of the elements between mass 23 (Na) and mass 238 (U). Three forms of asbestos fibre (actinolite, amosite and crocidolite) were distinguished from a non-asbestos control (wollastonite) based on their elemental profile, which demonstrated that LA-ICP-MS could be a viable technique for identification of asbestos fibres in clinical research samples.

In this study, two types of natural asbestos-like actinolite occurrences were sampled in order to understand their tectonic and metamorphic signification. Studied rocks were collected within two Variscan ophiolitic formations (Tréogat and Pont de Barel Formations, South Armorican Massif, Western France), mainly composed of amphibolites, and which recorded amphibolite to greenschist facies metamorphism. In these localities, the natural asbestos-like actinolite occurrences are closely related with the development of tectonic structures such as extension veins, tension gashes, σ and δ-type boudins. Field and petrostructural studies together with optical microscope, SEM and electron-microprobe analyses (EPMA) allowed to link early steps of the retrograde deformation event, during which acicular hornblende crystallizes in extension veins showing fuzzy boundaries or in hosting rock, with the late step of the same deformation event, during which hornblende is downgraded into asbestos-like actinolite synchronous with felsic melt circulation and tectonic structures opening. Field and microtectonic observations point to a sinistral strike-slip shearing for Pont de Barel formation and to a sinistral transtensive shearing for the Tréogat formation, which is consistent with the late regional variscan exhumation of the South Armorican Terrane. SEM observations show that asbestos-like actinolite originate from hornblende crystallographic plan fragmentation, starting first along the (110) plans and continue both along the (100) and (110) plans. EPMA analyses show that Na-Al-Si metasomatism is associated with this fragmentation. Temperature estimates of chlorite crystallization after hornblende are around 300°C for the Tréogat Formation and 200°C for the Pont de Barel Formation, suggesting that amphibole fragmentation can occur over a wide temperature range. Additionally, Principal Component Analysis was performed using crystallographic sites distribution. Results show a clear correlation between actinolite Si(T) and hornblende Al(T), Al(C) and Na(A) crystallographic sites, suggesting that asbestos-like actinolite after hornblende fragmentation is rather due to a decrease of pressure within the tectonic structures, as Al in amphibole is pressure-dependent. This decrease could be due to the fluid pressure, which is supra-lithostatic during tectonic structures opening.

As a potentially large Ag-Au epithermal deposit, Primorskoye comprises the following three areas: Kholodny, Spiridonych, and Teply. This deposit is located in the Omsukchan district of the Magadan Region, where similar deposits, including Dukat, Lunnoye, Goltsovoye, Arylakh, Tidit, and Perevalnoye, have developed. The deposit can be attributed to the Kalalagian volcano-tectonic depression and is localized in a flat-lying rock mass in the Late Cretaceous ignimbrites and rhyolites having thicknesses of greater than 700 m, which is cut through by numerous dykes of medium and major composition. According to the drilling data, the solid mass of leucocratic granites is located in deposits at a depth of 400–500 m with outcrops in the northeastern part of the ore field. The presence of Bi-containing galena and matildite, the availability of mid and high temperature facies of metasomatites (epidote and actinolite), and the specific physical and chemical conditions during the formation of the epithermal Ag-Au ores indicate the intrusive position above and the role of granitoids as generators of high temperature magmatic fluids, which introduced Bi and heated the rocks enclosing the mineralization. The geochemical features of the ores are well correlated with their mineral compositions. The high concentrations of Mn and Ag, elevated concentration of Au, low concentrations of Cu, Pb, Zn, Sb, As, Bi, and Te, low sum of REE, and negative Eu- and positive Се-anomalies were observed. The high values of the Te/Se, Sr/Ba, Y/Ho, and U/Th indicators in the ores are associated with the deposit location in the zone of granitoid massif effect. Further, the physical and chemical parameters of ore formation in the Teply area are unusual and are characterized by high temperatures, low concentrations of salts, and fluid density, which are indicative of the typical “dry steam” conditions. The obtained results allow the Primorskoye epithermal deposit to be attributed to the intermediate class. The information present in the article is practically valuable for the regional forecast and metallogenic developments as well as for searching and assessing the epithermal Ag-Au deposits.

Hydrothermal veins and dykelets that cross-cut layered olivine gabbros deep in the plutonic section of the Samail Ophiolite, Sultanate of Oman, point towards the occurrence of hydrothermal circulation in the deep oceanic crust, and these features record interactions between rock and high temperature seawater-derived fluids or brines. Deep penetration of seawater-derived fluids down to 100 m above the Moho transition zone and the consequent interactions with the host rock lead to hydrothermal alteration from granulite facies grading down to greenschist facies conditions. Here we present a study of veins and dykelets formed by hydrothermal interaction cutting layered gabbro in the Wadi Wariyah, using petrographic, microanalytical, isotopic, and structural methods. We focus on amphiboles, which show a conspicuous compositional variation from high-Ti magnesiohastingsite and pargasite via magnesiohornblende and edenite, to Cl-rich ferropargasite and hastingsite (up to 1.5 a.p.f.u. Cl) and actinolite. These minerals record a wide range of formation conditions from magmatic to hydrothermal, and reveal a complex history of interactions between rock and hydrothermal fluid or brine in a lower oceanic crustal setting. Large variations in Cl content and cation configurations in amphibole suggest formation in equilibrium with fluids of different salinities at variable fluid/rock ratios. The presence of subsolidus amphibole extremely enriched in chlorine implies phase separation and brine/rock interactions. 87Sr/86Sr values of 0.7031 to 0.7039 and stable δ18O isotopic compositions of 4.1 to 5.6‰ of the different amphibole types suggest a rock-dominated environment, i.e. with low fluid/rock ratios. However, the slight departure from mean Oman isotope values may indicate there was some influence of seawater in the aforementioned fluid-rock interactions. Our study provides new petrological data for the subsolidus evolution of gabbro-hosted amphibole-rich veins in the presence of a seawater-derived fluid.

Calc-alkaline lamprophyre dikes are hosted by tourmalinized metasedimentary rocks in the Northwest Territories, Canada. Some of these lamprophyre dikes are cross-cut by aplite and pegmatite dikes, as well as tourmaline-bearing quartz veins that were all derived from the nearby granitic O'Grady Batholith. The lamprophyre dikes are composed of actinolite to magnesio-hornblende, plagioclase, K-feldspar and quartz with minor phlogopite (up to 4.13 wt. % TiO2), titanite, apatite, pyrite, allanite-(Ce), and zircon. A zone near the margin of one of the dikes has been altered to tourmaline associated with actinolite to magnesio-hornblende, clinochlore, titanite and quartz, with minor clinopyroxene and apatite. Two generations of tourmaline are recognized: Tur I occurs in quartz at the margin of the dike and Tur II forms a massive aggregate with common inclusions of other minerals in an altered lamprophyre zone near the margin of the dike. The vast majority of the analyzed tourmaline is Al-deficient, with less than 6 apfu Al at the Z site (on average 5.691 apfu in Tur I and 5.601 apfu in Tur II). Tur I is mostly dravite with uvite, plus minor feruvite and fluor-uvite, while Tur II contains a greater proportion uvite, feruvite, and fluor-uvite. The most evolved tourmaline compositions observed are feruvite with up to 2.17 wt. % TiO2, and fluor-uvite with up to 0.84 wt. % F. The tourmaline composition reflects the unique geochemical environment in which it crystallized; from Tur I to Tur II, tourmaline becomes richer in Ca-, Fe-, and Ti, presumably due to the reaction of B-bearing fluids with the Al-poor, Ca-, Mg-Fe-, and Ti-bearing minerals in the lamprophyre dike. The high F contents of some tourmaline species suggest that it crystallized from fluids derived from the aplite and pegmatite dikes.

Asbestos is a naturally occurring silicate with six varieties from two groups of minerals serpentine (chrysotile) and five amphiboles (amosite, crocidolite, tremolite, anthrophyllite and actinolite...

Unusual series of hybrid metasomatic mineral zones are well developed when the granitic pegmatite veins cross-cut through ultramafic rocks at the Hafafit complex, South Eastern Desert of Egypt. Two groups of mineralogical zones are developed; the first group related to the serpentinized ultramafic rocks (peridotite-related zones) comprises anthophyllite-, actinolite- and vermiculite-bearing zones, whereas the second group related to the pegmatite veins (pegmatite-related zones) comprises hercynite- and corundum-bearing zones. Tourmaline-rich zone only occurs when the pegmatite veins come in contact between ultramafic rocks and biotite-rich granitic gneiss. The mineral assemblages, bulk rock geochemistry and in situ mineral chemistry suggest a metasomatic origin for the hybrid zones. The mineral assemblages: corundum + margarite ± Ca-plagioclase, hercynite + corundum + garnet ± chlorite, and anthophyllite + actinolite + enstatite, in addition to the constrained garnet-biotite/phlogopite geothermometer, and the higher tourmaline XMg, strongly indicate amphibolite facies metamorphism for the ultramafic-pegmatite hybrid zones. The constrained temperature ranges between 500 and 700 °C and a pressure around 7 kbars, with pronounced increases of metamorphism from the outermost zone in the serpentinized ultramafic ongoing to the pegmatite mineral zones. Juxtaposition of two contrasting rock types (highly reactive hot SiO2-, alkali-rich melt and cool silica-deficient ultramafic rocks) side by side would results in an intense contact bimetasomatic elemental exchange. The SiO2, H2O and alkalies would be offered by pegmatite melt, while MgO, FeO and CaO were supplied by serpentinized ultramafic rocks. The small volume of pegmatite melt relative to the ultramafic rocks would be easily desilicated by SiO2 diffusion into the ultramafic rocks to form the monomineralic SiO2-rich minerals in the peridotite-related zones. Consequently, Al2O3 would be concentrated in the residual melt to form corundum and other Al-rich mineral phases in the pegmatite-related zones. The small size of pegmatite veins and refractory nature of the ultramafic rocks could be the reasons precluding the formation of colored gem corundum in the Hafafit complex. Restricted occurrence of tourmaline-rich zone at the ultramafic-granitic gneiss contact is attributed to the diffusion of B-rich fluids generated from the leaching of biotite-rich granitic gneiss.

The Saghand Anomaly 5 is located in the Bafq-Saghand metallogenic province in the Central Iranian geostructural zone and contains Ti, REEs, Y, U, and Th mineralization. The mineralization is related to alkali-metasomatism and occurs in peripheral alteration zones around the iron ore deposits. Alkali-metasomatism and mineralization were controlled by tectonic activity along fault zones from ductile to brittle regimes of deformation. A metasomatic zoning is developed from outermost unaltered lithologies (subvolcanic diorite and quartz diorite host rocks) inwards to albite-actinolite metasomatite, phlogopite-actinolite metasomatite, and ultimately to magnetite orebodies. The last widespread hydrothermal event corresponds to an epidote2 ± chlorite ± calcite2 ± quartz paragenesis superimposed on all previous mineral associations. Microscopy studies reveal that ilmenite, davidite, allanite-(La), Ti–Y–U–Th-Oxide, REE-Oxide, rutile, and titanite and lesser amounts of thorite are ore minerals of Saghand Anomaly 5. The Ti–REE–Y–U–Th mineralization is related to Na–Ca-metasomatism and Ca-alteration and occurs as disseminated in albite-actinolite metasomatites and locally as veinlet-type in aplites and granites. The geochemical investigations indicate a calc-alkaline and continental-margin arc setting for granite and associated diorite-quartz diorite host rocks in the Saghand Anomaly 5. The REE patterns of the mineralized metasomatites show LREE enrichment and strong Eu negative anomalies. The presence of REE-rich hydrothermal phases suggests a significant mobilization and deposition of REEs, especially La, Ce and Y, by high temperature hydrothermal solutions within the Saghand Anomaly 5. The measured temperatures range from ∼748° to ∼766° C and ∼703° to ∼737° C for Na–Ca-metasomatic and K–Ca-metasomatic stages, respectively, using the magnetite1-actinolite and magnetite2-phlogopite oxygen isotope pairs, respectively. Both δD and δ18O values of actinolite and phlogopite indicate a magmatic source of actinolite and phlogopite forming fluids. In addition, C and O isotopic data of calcite2, from the late veinlets, indicate a magmatic origin of fluids in equilibrium with calcite2 and the formation temperature of 350 to 400° C.

The Se-Chahun Fe-P ore deposit is located in the Bafq mining district in the Central Iranian tectono-magmatic zone and contains REE and Th mineralization. The ore deposit consists of a magnetite-apatite massive ore that is significantly modified by late-stage metasomatic fluids that finally formed brecciated rocks within and at the margin of the ore deposit. Geochemical data from the rhyolitic rocks, Fe-P ore body and breccia as well as isotopic data from the breccia within the Se-Chahun Fe-P ore bodies, have been used to deduce the magmatic origin of the Fe-P ore zone and to assess the significance of post-magmatic processes with late-stage metasomatic fluids and the effects of these processes on remobilization of magmatic originated REE and concentration and deposition of Th. The chondrite-normalized REE patterns of the mineralized rocks in both the Fe-P ore and the Th mineralization zone demonstrate LREE enrichment and strongly negative Eu anomalies (Eu/Eu* = 0.25–0.91 for Th mineralization). δD and δ18O for actinolite paragenetic to Th-bearing silicates are estimated to be between −73.29 to −42.04 and 6.65 to 7.71, respectively, which lie within the both fields of magmatic and metamorphic fluids. Na-Ca metasomatism (which is evidenced by brecciation) has been a continuous process affecting the host rock, and the Fe-P ore body. Apatite, monazite, and Ti-La-Ce-Y-Nd-oxides are the main REE-bearing phases in the Fe-P ore body (REE≫Th) that are precipitated during magnetite crystallization whereas Th silicates (huttonite and thorite) occur within the breccia (Th ≫ REE) and were deposited from a late Th- and carbonate-rich fluid. Th mineralization occurred with late sodic-calcic fluids and Th-bearing minerals are paragenetic to actinolite, red albite, magnetite, titanite, calcite, and pyrite. Paragenetic association of Th minerals and actinolite, titanite, and calcite in carbonate veins and veinlets point to transportation of Th by carbonate complexes. The pH, fluid/rock ratio, Ca/Na ratio, and higher capability of Th (with respect to REE) in formation of carbonate complexes and lower concentration of Th (with respect to REE) in the source region are the most important geochemical parameters that triggered Th (Th ≫ REE) mineralization at the end of alkali metasomatism.

Los Guindos scheelite (±Zn, Bi, Sn, Ag) skarn presents mineral assemblages and a mineral chemistry similar to other worldwide strongly reduced W skarn deposits. Its reduced nature is defined based on the predominance of subcalcic garnets, Mo-free scheelite and absence of magnetite. Both the prograde and retrograde stages are evident at Los Guindos scheelite skarn. The prograde skarn is characterized by three zones: A zone I of garnet + helvine (Gr57Sps24Ad19Alm8 - Sps50Alm24Gr22Ad3; Grt + Hlv); a zone II of clinopyroxene + garnet (Di67Hd24Jo9 + Gr66Sps19Ad12Alm3; Cpx + Grt) and a zone III of garnet + vesuvianite (Gr73Ad22Sps3Alm2 - Gr58Sps22Ad10Alm9; Grt + Ves). Retrograde skarn is mainly represented by epidote - actinolite and minor F-rich actinolite (0.663 apfu of F) – potassium feldspar - chlorite (chamosite/clinochlore: ∼ 50/50) – muscovite – calcite - quartz. A hydrothermal stage developed in temporal continuity with retrograde skarn formed variable infilling associations of the following species: epidote – actinolite – scheelite – fluorite – calcite – quartz – sphalerite and chlorite. Scheelite mineralization process was triggered by an increase of Ca released during retrograde skarn replacements and was deposited during the following hydrothermal infilling stage. Other than sphalerite, minor bismuthinite and tetradymite, andorite, lillianite, gustavite, matildite and kësterite occur as hydrothermal associations after scheelite deposition. Scheelite-free reaction skarn preceding scheelite skarns was observed. Geobarometric calculations in this reaction skarn suggests an initial confining pressure of 2.5 kbar for the Los Guindos scheelite skarns. This pressure matches the estimated emplacement pressure of the Devonian-Carboniferous Achala batholith reported by previous authors. Geochemical correlation analyses suggest that this magmatism may have contributed mineralizing fluids channeled through regional structures and lithological contacts, causing infiltration metasomatism that originated scheelite (±Zn, Bi, Sn, Ag) mineralization in Cambrian and Ordovician country rocks. U-Pb analyses (LA-ICP-MS) of garnet in the Los Guindos scheelite skarn gave an age of 361 ± 11 Ma representing the age of the prograde stage of scheelite skarns and it should be framed within the Devonian-Carboniferous Metallogenic Epoch. Fil: Espeche, María José. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Museo de Mineralogía y Geología "Dr. A. Stelzner"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina Fil: Wan, Bo. Chinese Academy of Sciences; República de China Fil: Lira, Raul. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Museo de Mineralogía y Geología "Dr. A. Stelzner"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina Fil: Seltmann, Reimar. Natural History Museum; Reino Unido

El Romeral is one of the largest iron oxide-apatite (IOA) deposits in the Coastal Cordillera of northern Chile. The Cerro Principal magnetite ore body at El Romeral comprises massive magnetite intergrown with actinolite, with minor apatite, scapolite, and sulfides (pyrite ± chalcopyrite). Several generations of magnetite were identified by using a combination of optical and electron microscopy techniques. The main mineralization event is represented by zoned magnetite grains with inclusion-rich cores and inclusion-poor rims, which form the massive magnetite ore body. This main magnetite stage was followed by two late hydrothermal events that are represented by magnetite veinlets that crosscut the massive ore body and by disseminated magnetite in the andesite host rock and in the Romeral diorite. The sulfur stable isotope signature of the late hydrothermal sulfides indicates a magmatic origin for sulfur (δ34S between − 0.8 and 2.9‰), in agreement with previous δ34S data reported for other Chilean IOA and iron oxide-copper-gold deposits. New 40Ar/39Ar dating of actinolite associated with the main magnetite ore stage yielded ages of ca. 128 Ma, concordant within error with a U-Pb zircon age for the Romeral diorite (129.0 ± 0.9 Ma; mean square weighted deviation = 1.9, n = 28). The late hydrothermal magnetite-biotite mineralization is constrained at ca. 118 Ma by 40Ar/39Ar dating of secondary biotite. This potassic alteration is about 10 Ma younger than the main mineralization episode, and it may be related to post-mineralization dikes that crosscut and remobilize Fe from the main magnetite ore body. These data reveal a clear genetic association between magnetite ore formation, sulfide mineralization, and the diorite intrusion at El Romeral (at ~ 129 Ma), followed by a late and more restricted stage of hydrothermal alteration associated with the emplacement of post-ore dikes at ca. 118 Ma. Therefore, this new evidence supports a magmatic-hydrothermal model for the formation of IOA deposits in the Chilean Iron Belt, where the magnetite mineralization was sourced from intermediate magmas during the first Andean stage. In contrast, the beginning of the second Andean stage is characterized by shallow subduction and a compressive regime, which is represented in the district by the emplacement of the Punta de Piedra granite-granodiorite batholith (100 Ma) and marks the end of iron oxide-apatite deposit formation in the area.

Iron Oxide-Apatite deposits (IOA) have been found and investigated in the Tarom district, NW Iran. This area is a part of the Cenozoic Alborz-Azarbaijan magmatic belt in the foreland of the Arabia–Eurasia collision zone of the Alpine-Himalayan Orogen. In this region, volcanic and volcanoclastic rocks (Karaj Formation) are the main units which were later followed by the intrusion of late Eocene plutonic rocks. These intrusions are metaluminous I-type granitoids and have high-K calc-alkaline to shoshonitic affinity. The IOA deposits are mainly hosted by quartz monzonitic rock. These deposits occur as veins and veinlets with brecciated, banded and massive textures. Mineralogicaly, the IOA deposits are composed of magnetite, apatite, monazite, actinolite, clinopyroxene, pyrite, chalcopyrite, quartz and calcite. Rare earth element mineralization in the Tarom area is related to the IOA deposits. These elements are mainly concentrated in apatite crystals. Exploration studies indicate REE grades up to 1% in apatite crystals and up to 0.7% in the magnetite-apatite ore. These studies demonstrate that LREEs are more enriched compared to HREEs in magnetite-apatite ores, while actinolitic zones have less enrichment of LREE/HREE. Chondrite normalized REE patterns of IOA ores in the Tarom area are similar and show strong LREE/HREE fractionation and negative Eu anomaly. These similar REE patterns indicate that these units have a common origin. Magnetite-actinolite ores and actinolitic zones indicate flat patterns with low fractionation of LREE/HREE along with negative Eu anomaly. REE patterns of IOA deposits in Tarom area are similar to that of Kiruna-type Fe deposits. Furthermore, comparison of chondrite-normalized REE patterns of IOA ores with those of quartz monzonite host rock indicating very similar patterns. These similar patterns demonstrate that the mentioned quartz monzonitic intrusions and IOA deposits originated from a common magmatic source.

A tectonized ultramafic-mafic-pelitic package southwest of the Burgess Branch Fault Zone in the Rowe/Prospect Rock slice in Stockbridge, Vermont preserves Taconian subduction zone metamorphism. The polydeformed package consists of carbonatized and chloritized serpentinite lozenges that are faulted between graphitic phyllite and an intercalated zone of mafic greenstones and pelitic schists that retain primarily Taconian structures. Amphiboles zoned chemically in greenstones display decreases in PL (NaM4) and TK (AlVI + Fe3+ + 2Ti + Cr) from cores to rims. Pseudosection and amphibole isopleth calculations show that different greenstone bodies experienced peak subduction zone metamorphism at different depths between ∼19 and 32 Km (0.55–0.95 GPa) and/or at different temperatures between ∼425 and 500 °C. Barroisite and winchite cores preserve the highest pressure and lowest temperature peak metamorphism, which is interpreted as lower blueschist facies. All greenstones followed decompression cooling paths to lower greenschist facies where actinolite rims grew. Assembly of the ultramafic-mafic-pelitic package probably occurred in a Taconian exhumation channel containing mantle serpentinite, oceanic crust, and clastic rocks of the Laurentian margin and Iapetan Ocean basin.

The Ediacaran BISF at Hormuz Island is a newly identified glaciogenic iron-salt deposit in the Tethyan margin of Gondwana. The BISF was formed by synchronous riftogenic A-type submarine felsic volcanism and evaporate deposition. The mineralization occurs in a proximal felsic tuff cone and jaspilitic distal zones and contains 1 million tonne of hematite-rich ore with an average grade of 58% Fe. The ore structure shows cyclicity of macrobandings, mesobandings and microbandings of anhydrite, halite, hematite and chert, which marks a new record in BIFs geohistory. The alteration minerals in the proximal and distal zones are actinolite, ripidolite, epidote, sericite, tourmaline, clinochlore, anhydrite and clay minerals. The occurrence of metamorphosed polygenetic bullet-shape dropstones in BISF attests that there was probably a continuous process of ice melting, episodic submarine volcanism and exhalative hydrothermal banded iron salt formation during the Late Ediacaran time. The non-metamorphosed Neoproterozoic stratigraphy, the presence of genus Collenia, U-Pb dating (558 ± 7 Ma) and the marked negative δ13C excursion in cap carbonates are representative of Late Ediacaran glaciation, which has been identified worldwide. The REE+Y display light REE enrichment, unusually strong Tb-Tm anomaly, a weak positive Y anomaly, but no distinguished Eu and Ce anomalies, reflecting the glaciogenic nature of the BISF. The contents of Zr, Hf, Nb, Ta, Th, La, Ce and Y in BISF, dropstones, halite and cap carbonates are similar to those of the Neoproterozoic glaciogenic BIFs. Also, the Ni/Fe, P/Fe ratios and Fe/Ti – Al/Al + Fe + Mn + Ca + Na + K diagram suggest an exhalative hydrothermal Ediacaran-type BISF. The absence of brecciated magnetite in the ore association and the low contents of copper (9–493 ppm) and gold (

Primary ore-forming minerals retain geochemical signatures of magmatic crystallization information and can reveal the petrochemical conditions prevalent at the time of their formation. The Baogutu deposit is a typical reduced porphyry Cu deposit. Amphibole and biotite Fe 3+ /ΣFe ratios, minerals (feldspar, biotite, amphibole, zircon and apatite), in situ elemental and apatite Nd isotopic compositions were determined by Mossbauer spectroscopy, electron probe microanalysis, and laser ablation multiple-collection inductively coupled plasma mass spectrometry, respectively, to investigate the magma oxidation state, petrogenesis, source features, and to constrain the carbon species at magmatic stages for the intrusive phases. The results show that the primary plagioclase and amphibole in the mineralized diorite to granodiorite porphyry and post ore hornblende diorite porphyry are distinct (An 26-55 versus An 60-69 ; Mg-hornblende versus tschermakite). In particular, the amphibole shows distinct major and trace element compositions with light rare earth element enrichments and negative Eu anomalies in Mg-hornblende and light rare earth element depletions and no Eu anomalies in tschermakite. All the analyzed biotites are primary igneous phases with a biotite phenocryst profile showing significant variations of Zn, Cr, Sc and Sr from core to rim. These results may indicate the occurrence of mixing between two distinct magmas during mineral formation. Titanium in zircon and Si ∗ in amphibole thermometries indicate that magma crystallized at >900 °C and continued to ∼650 °C. In situ apatite Nd isotope (eNd(t) = 5.6–7.6, T DM2 = 620–460 Ma), indicate absence of significant reduced sedimentary contamination and the source of juvenile lower crust. Slightly decreasing Fe 3+ /ΣFe ratios from biotite and amphibole to whole rock indicate decreasing oxygen fugacity during magma crystallization. Recalculated biotite compositions according to Fe 3+ /ΣFe ratios indicate f O 2 values of less than Ni-NiO buffer (NNO) which show slightly lower values than that estimated according to zircon/melt distribution coefficients Ce anomalies (∼ΔNNO + 0.6). These values are consistent with the features of reduced porphyry Cu deposits. Crystallization of other mineral phases significantly affects the reliability of oxybarometer of zircon/melt distribution coefficients Eu anomalies and Mn contents in apatite. This oxidation state suggests that only CO 2 was present at the magmatic stage, and implies that CH 4 formed during CO 2 reduction occurring later hydrothermal alteration. The alteration of primary amphibole to actinolite released Ti, Al, Fe, Mn, Na and K to the fluid with later precipitation of titanite, albite and minor ilmenite and magnetite during actinolite alteration.

The Chadormalu is one of the largest known iron deposits in the Bafq metallogenic province in the Kashmar-Kerman belt, Central Iran. The deposit is hosted in Precambrian-Cambrian igneous rocks, represented by rhyolite, rhyodacite, granite, diorite, and diabasic dikes, as well as metamorphic rocks consisting of various schists. The host rocks experienced Na (albite), calcic (actinolite), and potassic (K-feldspar and biotite) hydrothermal alteration associated with the formation of magnetite–(apatite) bodies, which are characteristic of iron oxide copper-gold (IOCG) and iron oxide-apatite (IOA) systems. Iron ores, occurring as massive-type and vein-type bodies, consist of three main generations of magnetite, including primary, secondary, and recrystallized, which are chemically different. Apatite occurs as scattered irregular veinlets in various parts of the main massive ore-body, as well as apatite-magnetite veins and disseminated apatite grains in marginal parts of the deposit and in the immediate wall rocks. Minor pyrite occurs as a late phase in the iron ores. Chemical composition of magnetite is representative of an IOA or Kiruna-type deposit, which is consistent with other evidence. Whole rock geochemical data from various host rocks confirm the occurrence of Na, Ca, and K alteration consistent with the formation of albite, actinolite, and K-feldspar, respectively. The geochemical investigation also includes the nature of calc-alkaline igneous rocks, and helps elaborating on the spatial and temporal association, and possible contribution of mafic to felsic magmas to the evolution of ore-bearing hydrothermal fluids. Fluid inclusion studies on apatites from massive- and vein-type ores show a range of homogenization temperatures from 266 to 580 °C and 208–406 °C, and salinities from 0.5 to 10.7 wt.% and 0.3–24.4 wt.% NaCl equiv., respectively. The fluid inclusion data suggest the involvement of evolving fluids, from low salinity-high temperature, to high salinity-low temperature, in the formation of the massive- and vein-type ores, respectively. The δ34S values obtained for pyrite from various parts of the deposit range between +8.9 and +14.4‰ for massive ore and +18.7 to +21.5‰ for vein-type ore. A possible source of sulfur for the 34S-enriched pyrite would be originated from late Precambrian-early Cambrian marine sulfate, or fluids equilibrated with evaporitic sulfates. Field observations, ore mineral and alteration assemblages, coupled with lithogeochemical, fluid inclusion, and sulfur isotopic data suggest that an evolving fluid from magmatic dominated to surficial brine-rich fluid has contributed to the formation of the Chadormalu deposit. In the first stages of mineralization, magmatic derived fluids had a dominant role in the formation of the massive-type ores, whereas a later brine with higher δ34S contributed to the formation of the vein-type ores.

Metabasites belonging to the Arquia Complex and outcropping along the Pijao-Genova strip (western edge of the Central Cordillera of the Colombian Andes) consist of chlorite schists, actinolite schists with and without garnet, amphibolites, garnet-amphibolites, eclogites and metabasalts. Some bodies of serpentinized peridotites are observed along with metabasites. Both rock types are confined to the tectonic block bordered by the Cauca-Almaguer and Silvia-Pijao fault systems and their satellite faults. Metabasites were affected by a regional metamorphism, reaching their peak of metamorphism at the amphibolite facies. The Rare Earth Elements (REEs) (normalized to the C1 chondrite) from the studied rocks show a Light REEs depletion and a flat or no-fractionated Heavy REEs patterns. The metabasites´ REEs patterns, along with their La/Sm ratio < 0.6 and positive Nb, Ta and Ti anomalies, may suggest their protoliths are MORBtype related. The lithologic association between metabasites, few metapelites and deformed ultramafic rocks suggest that the rocks of the Complex Arquia can represent remnants of an ophiolite sequence of N-MORB type series. The whole rock-garnet Lu-Hf geochronology from metabasites yield an age of 128.7±3.5 Ma. This age has been interpreted as the age at which these rocks reached the eclogite facies, which in turn coincides with the roll-back process of the subducted ocean lithosphere and the Quebradagrande magmatic arc formation. Keywords: Petrology; metabasites; Arquia Complex; Cordillera Central; Colombia.

The Kaladawan Fe–Mo ore field in Altyn (Xinjiang Province, NW China) contains six Fe (–Mo) deposits, with total proven reserves of 60 Mt Fe and 10,000 t Mo. Tabular, lensoidal and stratiform orebodies occur in the Cambrian foliated marble, phyllite, carbonaceous slate, chlorite–sericite schist and quartz–sericite schist along the exocontact zone of the Kaladawan granite. Skarns are extensively developed and dominated by garnet, pyroxene, epidote, tremolite and actinolite, with minor chlorite, zoisite, quartz and calcite. Ore minerals are mainly magnetite and molybdenite. Five alteration and mineralization stages (I–V) were identified: the prograde (I) and retrograde (II) skarns are characterized by assemblages of garnet–pyroxene and epidote–tremolite–actinolite, respectively, intruded and replaced by mineral assemblages of magnetite–epidote–zoisite (III), quartz–sulfides (IV) and calcite–chlorite (V) in younging order. The Kaladawan garnet contains more andradite (61.2–94.4 mol%) than grossularite (37.5–5.0 mol%). Pyroxene is Mg-rich and Fe-poor, with an endmember range of 55.4–94.7 mol% diopside and 42.5–4.7 mol% hedenbergite. Amphibole comprises mainly tremolite and actinolite. The Kaladawan skarn mineral contents resemble typical skarn Fe and Mo deposits. In-situ LA-ICP-MS magnetite trace element analysis had identified unusually high Mg, Mo and Cr concentrations. The high Mo and the absence of molybdenite inclusions in magnetite suggest that the hydrothermal fluids may have been Mo-rich. The magnetite also contains similar (Ti + V) and (Al + Mn) values with typical skarn Fe deposits. Therefore, the Kaladawan Fe–Mo mineralization is best attributed to be skarn-type, and related to the Kaladawan granite intrusion.

The Half Dome Granodiorite, Yosemite National Park, California, is recognized in the field by euhedral, fresh-looking, black hornblende phenocrysts up to 2 cm in length. This variety of granodiorite typifies intermediate-age hornblende-phyric units of Cretaceous nested plutonic suites in the Sierra Nevada batholith. Although only inclusions of feldspar are evident in hand samples, the phenocrysts are riddled with up to 50% inclusions of every major mineral found in the host granodiorite plus metamorphic minerals formed during cooling. Amphibole compositions within single phenocrysts vary from actinolite with less than 1 wt% Al 2 O 3 to magnesiohornblende with over 8 wt%. Elemental zoning within the amphibole is highly irregular on the micrometer scale, showing patches and polygonal zones with dramatically different compositions separated by sharp to gradual transitions. The chemical compositions of entire phenocrysts are equivalent to hornblende plus a small proportion of biotite, suggesting that the non-biotite inclusions are the result of metamorphism of the phenocrysts. Backscattered electron imaging shows evidence of brecciation that may have been the result of volume changes as hornblende was converted to actinolite. Pressure calculations using the Al-in-hornblende barometer show unreasonably wide variations on the micrometer scale that cannot have been produced by temperature or pressure variations during crystallization. These hornblende phenocrysts would thus be unsuitable for geobarometry, and caution must be used to avoid similarly zoned phenocrysts in the application of the Al-in-hornblende geobarometer.