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Magmatic fluid degassing within shallow magma chambers underneath the ore bodies is critical to the formation of porphyry Cu-Au deposits (PCDs). Yet, it remains unclear how the fluid degassing influences the development of PCDs. Here, geochemical data of apatite, amphibole, and plagioclase from ore-bearing and coeval barren porphyries have been analyzed in Sanjiang metallogenic belt, China. The ore-bearing porphyries normally exhibit high and wide XF/XCl (31.76–548.12) and XF/XOH (0.779–7.370) ratios of apatites, which are evidently higher than those of the barren porphyries (XF/XCl of 1.03–26.58; XF/XOH of 0.686–3.602). Combined with the continuous variation features of Cl/OH ratios and H2O contents of melts calculated by amphiboles, as well as fluid migration models, we constrained the mechanisms of fluid degassing within shallow magma chambers underneath PCDs. There are three different ways of fluid degassing, while only fluid degassing via fluid channel stage can migrate and focus the metal-rich fluids effectively, conducive to the development of PCDs. The mechanisms of magmatic fluid degassing processes are further controlled by the storage depths of magma chambers and initial H2O contents of the magmas revealed by the compositions of amphibole, plagioclase, and thermodynamic modeling. Magmas with shallower storage depths and higher initial H2O contents are more likely to experience extensive and focused fluid degassing, leading to the generation of PCDs. This study demonstrates the potential utility of integrated mineral analyses and thermodynamic modeling for investigating the mechanisms of magmatic fluid degassing in porphyry systems, as well as for identifying prospective buried PCDs. [ABSTRACT FROM AUTHOR]

Several conceptual models have been proposed for the amalgamation of granitoid plutons, which range from incremental growth to single-stage emplacement of these systems. This diversity of views has led to intense debate about the thermomechanical state of silicic intrusions and the magma differentiation paths within the crust. In this contribution, we present a comprehensive petrologic, geochronologic, and magnetic fabric data set from the La Obra-Cerro Blanco intrusive suite, which allows us to explore the petrogenesis and magma emplacement processes in the upper crust. This intrusive suite is composed of (1) a vertically zoned granitoid intrusion in spatial association with mafic layers and stocks and (2) a cupola-like highsilica granite. We interpret this intrusive suite as assembled by diverse but coexisting intrusion mechanisms over a time span of ~1.4 m.y. from 21.4 to 19.9 Ma. As indicated by the subhorizontal magnetic lineation, the first stage was dominated by horizontal emplacement of sheet-like intrusions of intermediate compositions, which became increasingly silicic after plagioclase and amphibole fractionation throughout the crustal column. The latest stage was instead dominated by cooling, crystallization, and differentiation of a thickened granitoid body and the formation of a high-silica magma chamber. The steep magnetic lineation and the abundance of aplite and rhyolitic dikes observed in the cupola-like, high-silica granites suggest that this portion acted as an evacuation channel of high-silica magma toward shallower levels, offering a rare opportunity to understand not only silicic magma accumulation and storage in the upper crust, but also the processes connecting the plutonic and volcanic environments. [ABSTRACT FROM AUTHOR]

A multi-disciplinary approach of volcano-stratigraphy, petrology and geochemistry has shed light on the pre-eruptive processes, the eruptive triggering, behaviour and the architecture of the magma plumbing system during the explosive cycle of Petrazza at ca. 77–75 ka (PaleoStromboli I eruptive epoch, Stromboli). This was the largest magnitude eruptive cycle in Stromboli and one of the largest of the entire Aeolian archipelago, able to produce Vulcanian to sub-Plinian/Plinian phases with distal deposits found in the tephrostratigraphic record of the Tyrrhenian sea and surroundings. Our study highlighted that, differently from the present-day activity, the large magnitude Petrazza eruptive cycle could be attributed to phases of closed-system conditions, as also testified by the in equilibrium presence of amphibole, indicative of a "steady-state" magmatic status of the system. The explosive activity is then attributed to strong depressurization underwent by the plumbing system due to the cyclic closure/opening of the shallow conduit, possibly also in association with lateral collapse events. As shown by textural and compositional studies on plagioclase crystals, this decompression was also able to recall amphibole bearing mafic magma from the deep portion of the plumbing system (5–15 km of depth). [ABSTRACT FROM AUTHOR]

Alaskan-type ultramafic–mafic intrusions in convergent-margin settings provide valuable information on melt-cumulate petrogenetic processes operating at depth in the sub-arc crust. Here, we report the compositions and textural relationships of cumulus and postcumulus minerals in a suite of clinopyroxenites and hornblendites from the peripheral zone of the Tulameen Alaskan-type intrusion in British Columbia, Canada. Mineral chemistry is used to establish magma storage conditions (P, T, fO2, H2Omelt) and to reconstruct the composition of cryptic residual liquids that equilibrated with the mineral phases and subsequently escaped the local mush system. Residual liquids in equilibrium with clinopyroxene (diopside) are metaluminous calc-alkaline basalt to andesite; melts equilibrated with amphibole (magnesio-hastingsite) are metaluminous to peraluminous calc-alkaline dacite to low-silica rhyolite. Thermobarometry yields a robust estimate of storage pressure of 400 ± 50 MPa (~ 15 km paleodepth) for the Tulameen magma reservoir and equilibration temperatures of 1130–960 °C for clinopyroxene and 950–850 °C for amphibole. The large cooling interval between the early crystallization of clinopyroxene and late appearance and continued crystallization of peritectic amphibole facilitated progressive extraction of residual liquids from clinopyroxene-rich cumulates, consistent with textural relationships, mass balance calculations and experimental petrology. Peritectic dacitic melts are hydrous (~ 6–8.3 wt% H2Omelt), oxidized (fO2 ~ NNO + 1.6 to NNO + 3.6 log units) and buoyantly mobile with low density (~ 2200 kg/m3) and viscosity (~ 103 poise). Lower water contents likely reflect degassing of peritectic melts driven by amphibole crystallization; relatively high redox conditions are attributed to precursor fractionation of olivine and clinopyroxene preserved as cumulates in the core of the Tulameen intrusion. Peritectic amphibole crystallized in response to migration of a thermally buffered reaction front marking the stability limit of amphibole (≤ 950 °C) and driven by near-isobaric cooling. Pervasive infiltration of reactive dacitic liquids through the clinopyroxene mush formed intergranular/poikilitic amphibole and channelized flow was captured in part by cm-scale hornblendite segregations; aggregated melts formed in situ bodies of replacive hornblendite. The absence of orthopyroxene and rarity of plagioclase in the evolved ultramafic cumulates of Alaskan-type intrusions and similar arc-related rocks is attributed primarily to high H2Omelt and oxygen fugacity in differentiated arc magmas. [ABSTRACT FROM AUTHOR]

Amphibole and pyroxenes are the main reservoirs of rare earth elements (REEs) in the lithospheric mantle that has been affected by hydrous metasomatism. In this study, we developed semi-empirical models for REE partitioning between orthopyroxene and amphibole and between clinopyroxene and amphibole. These models were formulated on the basis of parameterized lattice strain models of mineral-melt REE partitioning for orthopyroxene, clinopyroxene, and amphibole, and they were calibrated using major element and REE data of amphibole and pyroxenes in natural mantle samples from intraplate settings. The mineral-melt REE partitioning models suggest that amphibole is not in equilibrium with coexisting pyroxenes in the mantle samples and that the amphibole crystallized at a lower temperature than that of the pyroxenes. We estimated the apparent amphibole crystallization temperature using major element compositions of the amphibole and established temperature- and composition-dependent models that can be used to predict apparent pyroxene-amphibole REE partition coefficients for amphibole-bearing peridotite and pyroxenite from intraplate lithospheric mantle. Apparent pyroxene-amphibole REE partition coefficients predicted by the models can be used to infer REE contents of amphibole from REE contents of coexisting pyroxenes. This is especially useful when the grain size of amphibole is too small for trace element analysis. [ABSTRACT FROM AUTHOR]

Five layers of detrital amphiboles in the CJ08-008 sediment core from the northwest Indian Ocean have been found. To analyze their genetic types and provenance, an electron probe microanalysis of 300 amphibole grains from the core was conducted to calculate the numerical and characteristic values of cations in the crystal structure. The results showed that amphiboles with high Si, Ca, and Mg contents and low Na and K contents exhibit a low degree of weathering and that amphiboles mainly comprise tschermakite (46.43~70.69%), followed by magnesiohornblende, in the calcic amphibole subgroup. The types of sources for these amphiboles are mainly different types of metamorphic and magmatic rock. A large proportion of the detrital amphiboles (>60%) are derived from metamorphic rocks, followed by intermediate acid-intrusive rocks. The genetic analysis of amphiboles showed that most of the medium acid-intrusive amphiboles belong to the crust–mantle type, followed by the mantle type. Most of the amphiboles of metamorphic origin are of the low-pressure type. The amphiboles in the CJ08-008 sediment core exhibit characteristics different from those brought by monsoons from surrounding land masses. The variations in the amphiboles indicate different sources, which may have different origins; these origins could include the Carlsberg Ridge, the Owen Fault Zone, or older submarine sediment sequences eroded by turbidity currents. [ABSTRACT FROM AUTHOR]

Non-classical pyriboles (NCPs) have tetrahedral silicate chains (Ibeam) of multiplicity higher than single (pyroxene) or double (amphibole) Ibeams and are known from amphiboles in altered mafic-ultramafic complexes. NCPs, their polysomatic sequences, and inherent chain-width disorder are petrogenetic tools for interpreting igneous and metamorphic processes. Magnetite, a refractory mineral that can trap and preserve NCPs is a major constituent of iron oxide-copper-gold (IOCG) deposits. We undertook a nanoscale study to show that NCPs and amphiboles are hosted within magnetite cores from the Jatobá Ni-bearing IOCG deposit, Carajás Mineral Province, Brazil. Monoclinic amphiboles and NCPs form polysomatic intergrowths or occur as sparse inclusions along {111}magnetite. There are two chemical populations of amphiboles: Mg-Fe- and Ca-(Al)-amphiboles, the latter including Ce-bearing Mg-hornblende and (ferro)tschermakite. The occurrence contains one of the widest ranges of chain silicates ever recorded, from simple intergrowths of single to triple Ibeam zippers, including pyroxene slabs, to longer NCP polysomes up to 15-Ibeam chains. Clinojimthompsonite (Cjim) is observed for the first time within magnetite. Although no discrete polysomes could be defined, the NCP-amphibole intergrowths have compositions between Mg-Fe amphiboles and Cjim based on Ibeam averages of 2.5–2.7. Relationships between increase in the number of C and A cations from amphibole (2-Ibeam) to n chain silicates (nIbeam) are formulated as nIbeam = T(2 + n) = C(5 + 3n) = A(1 + n), n = integer. Empirical models of crystal structures, validated by STEM simulation, are shown for 4- and 5-Ibeam chain silicates. Co-crystallization of double- and triple-chain silicate structures with rhythmic intergrowths as larger blocks along b is often accompanied by rhythmic Ca-Fe zonation along a, supporting primary NCP crystallization via self-patterning during amphibole growth within magnetite in a close-to-equilibrium system. Chain-width disorder is documented from defects including planar faults, derailments, jogs, and swells. Violations of zipper termination rules indicate primary growth rather than replacement. Amphibole-NCPs inclusions support a multi-stage evolution for Jatobá magnetite. They formed during the first cycle of magnetite overprinting within a mafic/ultramafic lithology that records syn-shearing events. Subsequent formation of calcic-amphiboles, including Ce-bearing species, indicate IOCG-related fluids at the onset of mineralization. (Ferro) tschermakite formed at ~7.5 kbar during high-pressure shearing is preserved during main ore deposition. The multi-stage amphibole-NCPs generations in magnetite revealed by our nanoscale study emphasize the interpretive value of magnetite for overprinting events in terranes with protracted geological histories. Analogous NCPs are likely to be abundant in magnetite from magmatic-hydrothermal deposits hosted by greenstone belts and altered mafic/ultramafic complexes. Likewise, discovery of Ce-rich hornblende provides new avenues to understand the early, alkali-calcic alteration stages of IOCG systems and models for REE incorporation into, and subsequent release from chain silicates. [ABSTRACT FROM AUTHOR]

Amphibole is an important mineral during the differentiation of arc magmas but rarely as a phenocryst in arc lavas or eruptive pyroclastic rocks. The Sanggeda complex, intruded into the ophiolite of the Indus–Yarlung Zangbo Suture Zone (IYZSZ), Zedong, southern Tibet, mainly consists of amphibole-rich, fine-grained, and porphyritic gabbros. The complex provides an opportunity to study the differentiation of arc magmas through amphibole crystals. Four distinct amphibole crystal populations can be recognized according to petrographic observations, EMPA, and LA–ICP–MS analysis. The first ones (Type 1) are fined-grained and euhedral, are crystallized during ascent, and are the product of the shallow emplacement of host magma. The second ones (Type 2) are euhedral, with slight negative Eu and Sr anomalies, and crystallize from an evolved magma that previously experienced plagioclase fractionation. Type 3 amphiboles have similar morphological characteristics to Type 2 but are without Eu and Sr anomalies. Type 4 crystals are shown as pseudomorphs, formed by the reaction–replacement between the clinopyroxene and melt. Type 1 crystals are autocrysts. Other amphiboles within host magma, whether presented as phenocrysts or cumulate nodules, are antecrysts. Based on the amphibole crystal population developed in the complex, in this study, a trans-crustal magma plumbing system is proposed, containing at least three magma reservoirs located at different crust depths: the shallow emplaced crust (~4.8 km), the mid-crust (~12.9 km), and the lower crust (~21.8–24.9 km). Early amphibole crystallization is an effective process to generate silicic residual melts. Gravity could help in that sense. Precursor amphibole and clinopyroxene can efficiently delaminate back into the mantle and promote the generation of silicic continental crust. [ABSTRACT FROM AUTHOR]

The Musovitsa Neolithic settlement mound is located near the village of Korten, in the Nova Zagora region, Sliven district. In geological context, it is situated in the Sredna Gora Zone. Most of the observed stone tools (predominantly chisels and adzes) are made of local materials that can be found in close proximity to the settlement area. One of them -- a tool made of ultrabasite, could be associated with the region of the Rhodopes Mountains or with the areas that refer to the crystalline basement of the Sredna Gora Zone. Another find -- a dark-olive green nephrite jade adze, showing traces of usage, is of special interest. It was found within an area, associated with the remains of a Neolithic dwelling, probably dating to the Karanovo II period. The nephrite jade raw-material is classified in the tremolite series of the amphiboles. Its traces of Co are coherent (45--47 ppm), but Cr (252--517 ppm) and Ni (693--980 ppm) show zoning which probably reflects the intensity of the green colouring. Nephrite jade tools are sporadically found in Bulgaria. Within the region of the Upper Thracian Plain the best parallels for the Neolithic artefact from Musovitsa are known from the Karanovo settlement mound. [ABSTRACT FROM AUTHOR]

The subduction-related Sunda-Banda arc hosts several giant and major Cu–Au–Mo porphyry and epithermal Au systems, making it one of the most important magmatic-related metallogenic belts in Indonesia. They are accompanied by a number of smaller systems, one of which is the recently discovered Randu-Kuning porphyry Cu-Au deposit on Java Island. The present study investigates the geochemical characteristics of this deposit through whole-rock and mineral geochemistry and mineral geothermobarometry, focusing on three sequential dioritic intrusions that make up the host igneous complex, two barren and the third mineralized. Moreover, a comparative analysis is performed between other porphyry deposits in the Sunda-Banda arc and with Grasberg in Papua. This study shows that the older porphyry deposits have mostly similar geochemical characteristics to the younger deposits, suggesting the same magma source, which is mantle-derived oxidized I-type magma. Amphibole geothermobarometry shows that the formation of syn-ore intrusion in the older porphyry was higher in temperature and pressure than those at the younger porphyry. The halogen and oxygen fugacities inferred from biotite and amphibole chemistry indicate an oxidized, water- and halogen-rich melt. Our study shows that combining amphibole and biotite chemistry and whole-rock geochemical data is useful to fingerprint the magmatic-hydrothermal processes, especially where multiple magmatic phases occur. This research also provides valuable insights into the magmatic-hydrothermal physiochemical conditions during the formation of the mineralized system. [ABSTRACT FROM AUTHOR]

Granulites and associated dykes from the less well-studied southern Ivrea–Verbano Zone (around Ivrea town) are characterized by combining field, macro, micro and chemical (major and trace-element mineral composition) data to identify chemical and rheological variations in the lower crust that could be relevant for geodynamic implications. The Ivrea granulites are similar to those in the Lower Mafic Complex of the central Ivrea–Verbano Zone. The mafic lithologies experienced stealth metasomatism (pargasitic amphibole and An-rich plagioclase) that occurred, at suprasolidus conditions, by a pervasive reactive porous flow of mantle-derived orogenic (hydrous) basaltic melts infiltrated along, relatively few, deformation-assisted channels. The chemical composition of the metasomatic melts is similar to that of melts infiltrating the central and northern Ivrea–Verbano Zone. This widespread metasomatism, inducing a massive regional hydration of the lowermost Southalpine mafic crust, promoted a plastic behavior in the lowermost part of the crust during the Early Mesozoic and, ultimately, the Triassic extension of the Variscan crust and the beginning of the Alpine cycle. [ABSTRACT FROM AUTHOR]

This study explores the capability of amphibole in tracing the physicochemical process of magma mixing through spatially associated gabbros, mafic microgranular enclaves (MMEs) and granodiorites from central Tibet. These rocks share similar zircon ages as well as zircon Hf‐O and plagioclase Sr isotopes. However, the amphiboles within the gabbros and granodiorites have different Sr and B isotope compositions, while amphiboles with both heterogeneous isotopic imprints occur in the MMEs. According to data and modeling, significant mixing of two isotopically distinct magmas is recorded by amphibole but not by zircon and plagioclase. Based on a synthesis of petrography, geochemistry and thermobarometry, we interpret this inconsistency by the crystallization order of minerals and propose that magma mixing occurred after the parent magma was emplaced at ∼10 km and cooled to ∼750°C. Our study highlights that amphibole may be a more sensitive tracer of magma mixing relative to other commonly used methods. Plain Language Summary: Magma mixing significantly shapes the composition of silicic igneous rocks representing the major constituent of the upper continental crust. Since bulk‐rock composition may only bear the average of mixed sources, in situ techniques such as Hf‐O isotopes in zircon and Sr‐Pb isotopes in plagioclase are widely used to investigate the details of magma mixing. However, these methods cannot constrain how magma mixing operates in the deep crust. This study novelly uses in situ Sr‐B isotopes and trace elements in amphibole to trace the physicochemical process of magma mixing through spatially associated gabbros, mafic microgranular enclaves and granodiorites from the central Tibetan Plateau. Our data show that significant mixing of two isotopically distinct magmas is recorded by amphibole but not by zircon and plagioclase. We demonstrate that the amphibole geochemistry (i.e., trace element, Sr‐B isotope compositions) may be more sensitive in tracing magma mixing relative to traditional isotopic tools and has the potential to unravel the physicochemical process(es) of magma mixing in the deep crust. In addition, our work reinforces the use of B isotopes in amphibole to discern the nature (fluids released from altered oceanic crust vs. residual slab) of the slab components that metasomatized the supra‐subduction mantle. Key Points: The amphiboles in central Tibetan magmatic complex have contrasting geochemical and Sr‐B isotopic compositionsSignificant magma mixing is well recorded by amphibole but not by zircon and plagioclaseAmphibole is a more sensitive tracer of magma mixing relative to zircon and plagioclase [ABSTRACT FROM AUTHOR]

The Dalaku'an mafic–ultramafic intrusion, located in the western segment of the East Kunlun, presents conducive conditions for the magmatic Cu-Ni sulfide deposits. According to the detailed petrographic observation, the amphiboles within distinct rock types were analyzed by EPMA analysis. The crystallization conditions, such as temperature, pressure, oxygen fugacity, and water content of the magma, were calculated to explore the genesis of the intrusion. The amphiboles were divided into three types: Amp-I, characterized by low silicon content but enrichment of aluminum, titanium, and alkali, predominantly comprising Tschermakitic hornblende and Magnesio-hornblende with mantle-derived traits; Amp-II, exhibiting elevated silicon content but diminished levels of aluminum, titanium, and alkali, primarily constituted of Magnesio-hornblende; whereas Amp-III manifests as Actinolitic hornblende, indicative of crustal origins. The calculated temperatures of amphiboles ranged between Amp-I (955–880) °C, Amp-II (852–774) °C, and Amp-III (761–760) °C; the pressures ranged between Amp-I (454–274) MPa, Amp-II (194–93) MPa, and Amp-III (101–84) MPa; the oxygen fugacities (△NNO) ranged between Amp-I (0.93–2.17), Amp-II (1.55–2.52), and Amp-III (1.89); and the water contents (H2Omelt) ranged from (6.69–8.67) to (5.90–7.32). The magma experienced multiple stages of crystallization and underwent complex magma evolution at different depths. The high oxygen fugacity and water content could be attributed to the subduction of the oceanic crust. The magma source of the Dalaku'an intrusion was metasomatized by fluids from subducting plates, thereby originating within a post-collision extension. [ABSTRACT FROM AUTHOR]

It has long been recognized that amphibole minerals, such as cleavage fragments of tremolite and anthophyllite, may exist in some talc deposits. We reviewed the current state of the science regarding the factors influencing mesotheliogenic potency of cleavage fragments, with emphasis on those that may co-occur in talc deposits, including dimensional and structural characteristics, animal toxicology, and the most well-studied cohort exposed to talc-associated cleavage fragments. Based on our review, multiple lines of scientific evidence demonstrate that inhaled cleavage fragments associated with talc do not pose a mesothelioma hazard. [ABSTRACT FROM AUTHOR]

The consumption of fluoride below the safe limit can result in dental caries, while high concentrations can lead to fluorosis, which can potentially impair the body's systems. One geological factor that influences the concentration of fluoride in water is the type of rock through which the water passes, including granite and its weathering products. The area is located within the Tandjungbuku Formation, which is predominantly composed of granite rock and contains several areas with Mining Business Permits (IUP) for commodities such as silica sand. This research serves as a form of mitigation in response to mining activities, post-mining, and the development of an industrial area. One anticipated impact is an increase in fluoride concentration in the research area, originating from both natural geological processes and human activities. The investigation involved geological mapping, petrographic analysis, XRD, and XRF analysis. Water sampling was conducted for both surface water and groundwater from wells in Resang Tandjungbuku Village. The research area consists of two rock units: granite, which acts as a non-aquifer layer, and colluvial deposits, which function as a free aquifer. Petrographic analysis identified minerals associated with fluoride, such as plagioclase, amphibole, and biotite. This was supported by XRD analysis with the presence of biotite, muscovite and kaoline minerals. XRF results revealed fluoride values in granite rock at 0.23% or 2,300 ppm, further confirming granite as a source of fluoride. Analysis of fluoride in surface water showed values ranging from 0.01 to 4.24 mg/L, while groundwater consistently had a value of 0.01 mg/L. [ABSTRACT FROM AUTHOR]

Olivine, the most abundant mineral in the upper mantle, exhibits elastic anisotropy. Understanding the seismic anisotropy and flow patterns in the upper mantle hinges on the crystallographic preferred orientation (CPO) of olivine. Similarly, hydrous minerals, which also display elastic anisotropy, play a crucial role in explaining seismic anisotropy in numerous subduction zones. High-temperature and -pressure simple shear experiments reveal that the CPO of amphibole can lead to significant seismic anisotropy. In this study, peridotite samples originating from the southern end of the Mariana Trench, commonly containing amphibole, were analyzed. The microdeformation fabric and seismic anisotropy were examined. The results indicate a weak fabric strength in olivine, yet identifiable deformation fabrics of A/D, D, and AG were observed. Various dislocation structures suggest that olivine experiences complex deformation across various temperatures. Not only can the original slip system transform, but the melt/fluid resulting from melting also has a substantial impact on the peridotite. Deformation precedes the melt/rock interaction, resulting in a strong melt/rock reaction under near-static conditions. Furthermore, the modal content of amphibole significantly alters the seismic anisotropy of peridotite. An increase in amphibole content (types I, III, and IV) enhances seismic anisotropy, particularly for type I amphibole. Notably, the presence of type I fabric amphibole promotes the Vs1 polarization direction parallel to the trench in subduction zones, a phenomenon observed in other subduction zones. Therefore, when considering mantle peridotite regions rich in amphibole, the impact of amphibole on seismic anisotropy must be accounted for. [ABSTRACT FROM AUTHOR]

This paper addresses the study of a pillow lava interbedded with Late Albian-Early Cenomanian sediments that crops out in Armintza (Bizkaia, Northern Spain). The lava flow is an alkaline basalt with abundant macrocrysts of clinopyroxene, kaersutite, Ca-rich plagioclase (50-86% An) and ilmenite, which display a variety of textures and complex zoning patterns indicative of open-system magmatic behaviour. Macrocryst cores are likely to be inherited antecrysts that underwent complex processes under deep pre-eruptive conditions (≈ 700-800 MPa). Microcrysts and macrocryst rims formed during magmatic ascent and emplacement at shallower levels (≈ 35 MPa). Hypothetical melts in equilibrium with clinopyroxenes and amphiboles have trace element compositions like metasomatic vein melts containing amphibole, and their patterns overlap with those of the Armintza pillow lava. This suggests a metasomatised lithospheric mantle with amphibole-rich veins as a potential source for the alkaline basaltic melt. It is even conceivable that the Armintza pillow lava and other alkaline volcanic manifestations of the Basque-Cantabrian Basin were part of the same magma plumbing system through which a series of time-limited eruptions of different batches of magma ascended from the lithospheric mantle to the upper crust during the Albian to the Santonian. [ABSTRACT FROM AUTHOR]

Substitution of chlorine for hydroxyls in calcium amphiboles has been widely documented, but the effect of this substitution on thermal stability is not known. Experimental reversal data are presented here comparing the upper-thermal stability of amphiboles formed in the ferro-pargasite and ferro-chloro-pargasite bulk compositions. Experiments were made over the range of 550–900 °C and 0.5–3 kbar at oxygen fugacities of log(fO2) of –0.3 to +0.5 relative to Co-CoO. Electron microprobe analysis of amphiboles made from the ferro-pargasite bulk composition were found to be ferro-pargasite, while those made from the ferro-chloro-pargasite bulk composition were low in A-site Na and Cl and were better classified as Cl-bearing ferro-ferri-hornblende. Although the differences between desired and observed amphibole compositions complicate the comparison of their thermal stabilities, it can be deduced that the Cl-bearing amphibole has a steeper dP/dT slope and, above 1 kbar, a lower thermal stability than ferro-pargasite. Thermodynamic analysis of the Cl-bearing amphibole was also done to extract thermochemical data for the Cl end-member amphibole ferro-chloro-hornblende [Ca2(Fe4Al) (AlSi7)O22Cl2 = Fe-Cl-Horn] that are consistent with the thermodynamic database of Holland and Powell (2011). Using an ideal-activity expression and estimated values for the heat capacity (CP = 1.106 + 8.9156 × 10−5(T, K) – 11218.3/T2 − 5.9548/T0.5; kJ/K·mol) and volume (283.0 ± 1.5 cm3/mol) for Fe-Cl-Hom, the derived values for (Δ H f o) and S ° are −10 842.6 ± 10.3 kJ/mol and 618.8 ± 11.1.J/K·mol. respectively. The implication of this work is that (1) chlorine appears to lower the thermal stability of a given calcium amphibole in contrast to the marked increase in thermal stabilities caused by fluorine, and (2) thermochemical data such as those derived in this study allow absolute concentrations of chloride salts to be calculated in metasomatic paleobrines, as illustrated for the Bamble sector of southern Norway reported in the literature. [ABSTRACT FROM AUTHOR]

Magnesio-ferri-hornblende, ideally □Ca2(Mg4Fe3+)[(Si7Al)O22](OH)2, is a new mineral of the amphibole supergroup from the Husite granitic complex related to skarn-type Fe-Cu mineralization in the Western Tianshan, Xinjiang, northwestern China. The new species and the new name have been approved by the IMA-CNMNC (2021-100). Magnesio-ferri-hornblende is dark green to green-black with a vitreous luster and a pale gray-green to gray-white streak. It occurs mostly as subhedral-columnar crystals with lengths of 0.5 to 3 mm and shows well-developed {110} cleavage. It has a Mohs hardness of ~5 and a Vickers microhardness of 389–448 kg/mm2 (VHN load in 100 g) and is brittle with a conchoidal fracture. The measured and calculated densities are 3.275(6) and 3.204 g/cm3, respectively. In transmitted plane-polarized light, magnesio-ferri-hornblende is strongly pleochroic, X = pale yellow, Y = yellowish brown, Z = dark yellowish green. It is biaxial (−), α = 1.651(2), β = 1.658(2), γ = 1.662(2), 2V (meas) = 73 (1)° to 82 (1)°, and 2V (calc) = 73.9 (1)°, dispersion is r > v, medium to strong. The orientation is Y||b, X^a = 31.5° (β obtuse), Z^c = 16.5° (β acute). Magnesio-ferri-hornblende is monoclinic, space group C2/m, a = 9.8620(3), b = 18.1060(5), c = 5.30810(10) Å, β = 104.8480(10)°, V = 916.17(4) Å3, Z = 2. The seven strongest lines in the powder X-ray diffraction pattern are [d in Å(I)(hkl)]: 8.397(52)(110), 3.383(41)(150), 2.717(100)(151), 2.597(84)(061), 2.545 (61)(20 2), 1.854(49)(1 7 2), and 1.519(62)(6 2 2). Analysis by a combination of electron microprobe and Mössbauer spectroscopy gave SiO2 47.37, TiO2 1.51, Al2O3 7.07, Fe2O3 3.86, FeO 11.62, MgO 12.77, CaO 11.22, SrO 0.15, MnO 0.39, Na2O 1.54, K2O 0.78, Cl 0.15, F 0, H2Ocalc 2.01, Cl=O −0.03, sum 100.41 wt%. The empirical formula calculated on the basis of 24 (O+OH+F+Cl) with (QH+F+Cl) = 2 apfu is A(□0.62Na0.23K0.15)Σ1.00B(Ca1.76Na0.21Mn0.02Sr0.01)Σ2.00 C (M g 2.79 F e 1.42 2 + F e 0.43 3 + T i 0.17 A l 0.16 M n 0.03 ) Σ 5.00 T (S i 6.94 A l 1.06 ) Σ 8.00 O 22 W (O H 1.96 C l 0.04 ) Σ 2.00. The crystal structure of magnesio-ferri-hornblende was refined to an R1 of 3.95% using 2185 data (>2σ) collected with MoKα X-radiation. The A site is dominantly occupied by □ where A(Na+K+2Ca) ≥0.5. TAl is ordered at the T(1) site. M(1) and M(3) are dominantly occupied by Mg2+, and M(2) is occupied by both Mg2+ and high-charged cations. The new mineral occurs most commonly in the porphyry-skarn Fe-Cu-Mo-Au- and hydrothermal Au-mineralized granitoids with high oxygen fugacity but is rare or absent in barren intrusions. Its finding has important significance for magma fertility discrimination and can potentially be used in regional exploration for porphyry-skarn ore systems. [ABSTRACT FROM AUTHOR]

The main focus of studying sediment sources in marine areas is to determine the properties of clastic minerals originating from different rivers. Variations in the characteristics of clastic minerals occur due to differences in the types of source rocks within the watershed. Determining the source rock of clastic minerals in the marine area can improve the accuracy of provenance analysis. Electron probe microanalysis of 258 amphibole grains from six surface stations in the South Yellow Sea (SYS) was conducted to calculate the numerical and characteristic values of cations in the crystal structure. The results showed that amphibole in the SYS is mainly magnesiohornblende (52.2% ~ 81.4%) in the calcic amphibole subgroup, followed by tschermakite. The source rock types of amphibole are mainly different types of magmatic (ultrabasic, basic, and intermediate acidic) and metamorphic rocks. Amphibole derived from intermediate-acid intrusive rocks accounts for a large proportion (>40%). The genetic analysis of clastic amphibole in the SYS showed that most of the medium-acid invading amphibole belong to crust-mantle type, followed by mantle type. Most of the amphibole from metamorphic origins are of medium-low pressure type (± 80%). Combined with electron probe analysis of amphibole from the Huanghe River (the Yellow River, HH) and Changjiang River (the Yangtze River, CJ), the amphibole in the SYS exhibits characteristics inherited from these two rivers. The northern sea area has a strong resemblance to the sediments from the HH, while the southern area is more influenced by sediments supply from the CJ. The central area represents a mixed zone with a higher sediment supply from the HH. The clastic amphibole deduces the type of source rock in different watersheds, serving as a crucial link between the source rock, watershed, and marine area, providing a basis for provenance analysis. [ABSTRACT FROM AUTHOR]

Tectonic slices of greenschist – epidote blueschist – epidote amphibole schist – garnet epidote amphibole schist are exposed in the northern part of the NOC. Metamorphic P-T conditions and P-T paths of the garnet epidote amphibole schist and epidote blueschist were determined with the help of pseudosection calculations in the MnNCKFMASHTO system using the software Perple_X. The garnet epidote amphibole schist records a pre-peak metamorphic stage at ~12 kbar and ~360°C in the lawsonite blueschist facies field. Lawsonite and glaucophane are not preserved in the rock and are attributed to progressive metamorphic reactions during prograde metamorphism. The peak metamorphic stage is constrained at ~14 kbar and ~570°C in the hornblende eclogite facies field. Post-peak metamorphism shows slight cooling and decompression from ~550°C and ~13 kbar, possibly down to ~350°C and ~7 kbar in the greenschist facies field. These three metamorphic stages reveal a clockwise metamorphic P-T path of evolution for the garnet epidote amphibole schist. The geotherm at metamorphic peak P-T condition is ~12.5°C/km, which is hotter by ~350°C compared to thermal models of mature subduction zones but shows good agreement with models of warm subduction zones. Therefore, the low geothermal gradient of ~8°C/km during the prograde metamorphism possibly reflects the subduction of cold Neo-Tethyan ocean crust when the temperature conditions of the subduction zone were still warm. The epidote blueschist shows peak metamorphism at ~10 kbar and 380°C with a clockwise P-T path. It indicates metamorphism at a more mature stage of subduction. Buoyancy-driven exhumation along the subduction channel due to the serpentinization of the upper mantle wedge played a vital role in the detachment and exhumation of the tectonic slivers of metamorphic rocks from different depth sections in the northern margin of the NOC. [ABSTRACT FROM AUTHOR]

The mechanisms governing a commonly observed seismic velocity drop in the cratonic lithosphere, referred to as the mid‐lithospheric discontinuity (MLD), have been widely debated. To identify the composition and seismic structure of MLDs, we have analyzed Sp receiver functions (SRF) and mantle xenocrysts for six regions across Australia. We utilize locations where seismic stations and kimberlite‐hosted mantle xenocrysts are both available, allowing for comparison between seismological and petrological constraints. Our results show negative SRF phases indicative of the MLD coincide with clinopyroxene‐depleted zones at 60–140 km depth. Clinopyroxenes with different chemical compositions across the MLD define a litho‐chemical discontinuity. Modeling and experimental data show that MLDs may be explained by modified lherzolite with 10%–20% modal pargasite. Pargasite MLDs may form when rising H2O‐bearing melts cross the amphibole dehydration curve and react with clinopyroxene in lherzolite. Because the amphibole dehydration curve is isobaric at 80–120 km, pargasite will be precipitated as horizontal channels. Plain Language Summary: Seismic imaging of Earth's lithosphere has revealed a seismic velocity drop at 60–120 km depth, termed the mid‐lithosphere discontinuity (MLD). The mechanisms governing the MLD have been extensively debated. To advance the understanding of the MLD we carried out an interdisciplinary study to investigate the seismic structure and composition of MLDs identified in the cratonic lithosphere of Australia. We integrated analysis of seismic converted signals from discontinuities recorded by permanent seismometers with geochemical data for kimberlite‐hosted mantle xenocrysts collected in the vicinity. The method allows direct comparison between seismological and petrological constraints. Our results suggest that the MLD comprises anomalously low abundances of clinopyroxene and separates geochemically distinct layers within the lithospheric mantle. Experimental results and modeling suggests that the observed decrease in seismic velocity and absence of clinopyroxene may relate to the formation of pargasite channels in modified lherzolite. Key Points: Sp receiver functions and mantle xenocrysts are used to study mid‐lithosphere discontinuities beneath Australian cratonsMid‐lithosphere discontinuity at 60–120 km depth corresponds with mantle xenocryst populations that are depleted in clinopyroxeneModeling and experimental data suggests the mid‐lithosphere discontinuity is caused by pargasite‐bearing lherzolite [ABSTRACT FROM AUTHOR]

Water is known to play a crucial role in the generation of many large igneous provinces (LIP) worldwide, but the amount and origin of the water in their sources is still under debate. To address this question, this paper presents in situ major-, trace-element, and Sr isotope data coupled with bulk-mineral O-HHe isotope analyses of amphibole in a suite of aillikites from the Tarim LIP (NW China). The cores of zoned macrocrysts and microcrysts display partially overlapping compositions ranging between edenite and pargasite (75-83 versus 75-80 Mg#), which suggest a common origin from an evolving magma. The rims (Mg# = 75-80) of both macrocrysts and microcrysts are very similar to their cores for many elements, except for higher Sr and Ba contents. All the amphibole zones show similar primitive mantle-normalized trace element patterns, suggesting that they crystallized at different stages during magmatic evolution. This interpretation is confirmed by the homogenous Sr isotope compositions (87Sr/86Sr(i) = 0.70298-0.70394) of these amphiboles, which overlap with those of magmatic apatites and perovskites in these aillikites. The hydrogen isotope compositions (-D = -120‰ to -140‰) of the amphiboles are significantly lower than average mantle values. Given the low water contents (<0.66 wt%) of these minerals, the low H iso signatures of the amphiboles might be caused by variable H2O loss during magma ascent. However, open-system Rayleigh fractionation modeling suggests that the hydrogen isotope compositions of these amphibole phenocrysts cannot be fully reproduced by crystallization following magmatic degassing. These low Î'D values require incorporation of recycled altered oceanic crust containing hydrous components in the plume source of these aillikites, which is consistent with the previously published moderately radiogenic He isotope ratios of olivine separates and bulk-rock Os and Pb isotope data for these same samples. We conclude that water in these magmas was derived from a plume source containing recycled water-bearing oceanic crust. [ABSTRACT FROM AUTHOR]

Identifying ultrahigh-temperature (UHT) metamorphism in basic granulites is challenged by the uncertainty of peak temperatures. Consequently, available temperature indicators are desiderated all along. In this study, we investigated low-pressure basic granulites from the Daqingshan, North China Craton and determined a UHT peak condition around 1000–1050 °C and 0.8–0.9 GPa. This peak condition was constrained by combining the AlT of 0.10–0.12 in clinopyroxene (Cpx) cores, maximum Ti of 0.36–0.38 in amphibole (Amp) cores and anorthite proportion (X An) of 0.67–0.70 and 0.61–0.63 in plagioclase (Pl) cores/mantles analyzed in two selected samples. The P – T records obtained from several thermobarometers related to amphibole, plagioclase and/or clinopyroxene were also verified to be in agreement with the phase equilibria modeling results. Notably, AlT-in-Cpx is assessed to be a reliable temperature indicator in basic granulites with the Opx–Cpx–Pl–Amp assemblage, albeit could be influenced by bulk-rock compositions in some extent and has a temperature standard error of ~70 °C. Besides, the post-peak evolution was dominated by near-isobaric cooling at 1.94–1.93 Ga, to a fluid-absent solidus as high as ~940 °C. During the cooling process, plagioclase and amphibole grew together at the expense of Al-rich clinopyroxene and unsegregated melts, accompanied by the (rimward) decrease of AlT-in-Cpx, Ti-in-Amp and X An-in-Pl. A pre-peak process is inferred to be decompressional heating. The UHT metamorphism in Daqingshan is interpreted to result from asthenosphere upwelling and thermal advection from regional mantle-derived magmatism during post-orogenic extension, in a newly developed back-arc-related environment. [ABSTRACT FROM AUTHOR]

The major- and trace-element compositions of amphiboles in andesite from Quaternary Yufu Volcano, northeastern Kyushu, Japan were analysed to investigate the generation processes of andesitic magma from Yufu Volcano. The amphiboles in andesite from Yufu volcano can be divided into two groups based on major-element composition: pargasite and magnesio-hornblende. To estimate temperature, pressure, and major- and trace-element compositions of melts in equilibrium with amphiboles, we used the recently proposed methods that can calculate temperature, pressure, major element compositions, and partition coefficients of trace-element between amphibole and melt using only the major-element compositions of amphibole. The estimated temperature, pressure, and major-element composition of melt in equilibrium with the amphibole phenocrysts indicate that each group crystallised under different conditions. These differences suggest that two magma chambers at different depths existed beneath Yufu Volcano and that the andesitic magma of Yufu Volcano was formed by mixing of the two magmas. The trace-element compositions of melts in equilibrium with the pargasite and magnesio-hornblende, estimated by applying the partition coefficients calculated from major-element compositions of amphibole to trace-element compositions of amphiboles, indicate magma derived from slab melt and the partial melting of crustal material, respectively. Because magma is a mixture of minerals and melt, we estimate the chemical compositional ranges of the two end-member magmas on the Y versus SiO2 diagram from the mixing relationship between amphibole and estimated melt, as well as phenocrysts of plagioclase, clinopyroxene, and orthopyroxene. The overlap of the estimated compositional range with the trend of whole-rock composition represents the chemical compositions of the end-members of magma mixing, yielding estimates of the mafic (SiO2 ≈ 45 wt %) and felsic (SiO2 ≈ 68 wt %) end-member magmas. Furthermore, we estimate the concentrations of other elements in the end-member magmas by substituting the estimated SiO2 concentrations of the magmas into linear regression equations between the whole-rock contents of other elements and SiO2. The trace-element compositions of the mafic and felsic end-member magmas, as estimated in this study, have similar features to those of gabbroids and Cretaceous granitic rocks, respectively, that are presumed to lie beneath Yufu Volcano. These similarities could be explained by the possibility that the compositions of the end-member magmas were influenced by basement rocks. [ABSTRACT FROM AUTHOR]

The paper presents data on the formation of K–Na richterite in the enstatite + diopside association with K2CO3–Na2CO3–CO2–H2O fluid at 3 GPa and 1000°C as a model for the formation of this mineral in peridotites of the upper mantle. Richterite formation depends on the (H2O + CO2)/(K2CO3 + Na2CO3) and K2CO3/Na2CO3 ratios in the starting material. A high concentration of alkaline components in the fluid leads to the decomposition of clinopyroxene, the formation of olivine, and a change in the component composition of the pyroxene and amphibole. Fluids with a high potassium concentration are favorable for the formation of K-richterite similar in composition to that formed in metasomatized peridotites of the upper mantle. In some cases, such a fluid leads to the decomposition of amphibole and stabilization of alkaline melt. An increase in the activity of the sodium component results in richterite similar in composition to richterite from lamproites. The clarified relations can be used to assess the activities of fluid components and conditions for the formation of K-richterite. To update the data bank of the Raman spectra of minerals, the largest and most homogeneous amphibole crystals of different compositions were studied. [ABSTRACT FROM AUTHOR]

Ferry-kaersutite as a rare mineral have been found in North-Western part of the Ukrainian Shield where alkalineultrabasic rocks of jacupirangite-melteigite series are widespread. Ferry-kaersutite occurs in essexite that form thin veins and apophyses from dikes of porphyry-like alkaline-ultrabasic rocks. By results of microprobe analyses ferrykaersutites are of such composition (%): 39—40 SiO2; 4.6—5.07 TiO2; 14.6—14.9 Al2O3; 16.9—18.4 FeOtot; 7.95— 8.09 MgO; 10.5—11.0 CaO; 2.4—2.9 Na2O; 2.7—2.9 K2O. In alkaline-ultrabasic rocks of this region different more magnesian amphiboles (pargasites, richterites, magnesio-riebeckite, katophorite and other intermediate varieties) are present. Some of these amphiboles are enriched in TiO2 (to 2.9—3.2%). It is assumed that studied ferry-kaersutite has formed at quick crystallization and partly contamination of alkaline-ultrabasic melts in veins and apophyses among country granitoids. [ABSTRACT FROM AUTHOR]

Metasomatized mantle xenoliths containing hydrous minerals, such as amphiboles, serpentine, and phlogopite, likely represent the potential mineralogical compositions of the metasomatized upper mantle, where low seismic velocities are commonly observed. This study presents the first experimentally determined single‐crystal elasticity model of an Fe‐free near Ca, Mg‐endmember amphibole tremolite at high pressure and/or temperature conditions (maximum pressure 7.3(1) GPa, maximum temperature 700 K) using Brillouin spectroscopy. We found that sound velocities of amphiboles strongly depend on the Fe content. We then calculated the sound velocities of 441 hydrous‐mineral‐bearing mantle xenoliths collected around the globe, and quantitatively evaluated the roles that amphiboles, phlogopite and serpentine played in producing the low velocity anomalies in the metasomatized upper mantle. Plain Language Summary: Amphiboles are the most widely distributed hydrous minerals resulting from metasomatism in the upper most mantle. We measured sound velocities of tremolite (Ca, Mg endmember of the amphibole series) at high pressures and high temperatures by Brillouin spectroscopy. Based on global hydrous‐mineral‐bearing mantle xenoliths record, we quantitively evaluated the contributions of amphiboles, serpentine, and phlogopite to low velocity anomalies and water storage in the upper most mantle. We found the existence of hydrous minerals (amphiboles, serpentine, and phlogopite) remains a viable explanation for the low velocity anomalies in the upper most mantle (e.g., mid‐lithosphere discontinuity). Compared to serpentine and phlogopite, although the amount of velocity reduction caused by amphibolization is moderate, the formation of amphiboles does not require K, Al, Si‐rich environments like phlogopite, or exceedingly water‐rich environments like serpentine. Key Points: The single‐crystal elasticity of tremolite is determined by Brillouin spectroscopy up to 7.3 GPa and 700 KSound velocities of uppermost mantle amphiboles mainly depend on Fe contentHydrous minerals (amphiboles, serpentine, phlogopite) are plausible causes of the low velocity anomalies in the uppermost mantle [ABSTRACT FROM AUTHOR]

Exploitable or potentially exploitable deposits of critical metals, such as rare-earth (REE) and high-field-strength elements (HFSE), are commonly associated with alkaline or peralkaline igneous rocks. However, the origin, transport and concentration of these metals in peralkaline systems remains poorly understood. This study presents the results of a mineralogical and geochemical investigation of the Na-metasomatism of alkali amphiboles and clinopyroxenes from a barren peralkaline granite pluton in NE China, to assess the remobilization and redistribution of REE and HFSE during magmatic-hydrothermal evolution. Alkali amphiboles and aegirine-augites from the peralkaline granites show evolutionary trends from sodic-calcic to sodic compositions, with increasing REE and HFSE concentrations as a function of increasing Na-index [Na#, defined as molar Na/(Na + Ca) ratios]. The Na-amphiboles (i.e., arfvedsonite) and aegirine-augites can be subsequently altered, or breakdown, to form hydrothermal aegirine during late- or post-magmatic alteration. Representative compositions analyzed by insitu LA-ICPMS show that the primary aegirine-augites have high and variable REE (2194-3627 ppm) and HFSE (4194-16,862 ppm) contents, suggesting that these critical metals can be scavenged by alkali amphiboles and aegirine-augites. Compared to the primary aegirine-augites, the presentative early replacement aegirine (Aeg-I, Na# = 0.91-0.94) has notably lower REE (1484-1972) and HFSE (4351-5621) contents. In contrast, the late hydrothermal aegirine (Aeg-II, Na# = 0.92-0.96) has significantly lower REE (317-456 ppm) and HFSE (6.44-72.2 ppm) contents. Given that the increasing Na# from aegirine-augites to hydrothermal aegirines likely resulted from Na-metasomatism, a scavenging-release model can explain the remobilization of REE and HFSE in peralkaline granitic systems. The scavenging and release of REE and HFSE by Na-metasomatism provides key insights into the genesis of globally significant REE and HFSE deposits. The high Na-index of the hydrothermal aegirine might be useful as a geochemical indicator in the exploration for these critical-metals. [ABSTRACT FROM AUTHOR]

The Ozren ophiolite complex (OOC) of the Dinaridic Ophiolite Belt is one of the six ophiolite complexes in Bosnia and Herzegovina. This paper deals with the mineral chemistry of amphiboles determined by electron probe micro-analysis and micro-Raman spectroscopy. The detected amphibole generations and types in mafic, ultramafic, and metamorphic rocks suggest a polystage evolution and are therefore useful petrogenetic indicators of the investigated OOC. Most gabbroic rocks and dolerites contain primary magmatic amphibole1 (magnesio-hornblende to pargasite, occasionally hastingsite) and prismatic to needle-like aggregates of late magmatic amphibole2 (magnesio-hornblende), while plagiogranite contains ferri-winchite and ferro-ferri-winchite as primary magmatic amphibole. Post-magmatic amphiboles were detected in dolerites, troctolites, and lesser in peridotites. The Na-(Ti)-rich amphibole3 (ferri-winchite and ferro-ferri-winchite to katophorite and ferri-katophorite) with amphibole4 (grunerite) rim formed along the grain boundaries of clinopyroxene, amphibole1, and plagioclase in dolerites. A part of these amphiboles grows into amphibole1, 2. Kaersutite to ferri-kaersutite, associated with phlogopite, occur in troctolites and dunites, while Mhbl was detected in harzburgite. The ultramafic rocks (lherzolites, harzburgites, and dunites) and the gabbroic layer are crosscut by clinopyroxene–plagioclase gabbroic and clinopyroxene–plagioclase–amphibole gabbro–dolerite dykes, suggesting 'dry' and 'hydrated' percolating melts generated in inferred subridge and supra-subduction settings, respectively. The amphibole3 and 4 in gabbros and dolerites and similar amphibole types in ultramafic rocks could be related to inferred arc-type basaltic and plagiogranitic percolating melts and fluids. Low-Al amphibole5 (tremolite and actinolite) and associated chlorite, albite, and clinozoisite represent the ocean-floor alterations in mafic rocks. Amphibole6 (magnesio-hornblende to pargasite) was identified in metamorphic sole amphibolites. Micro-Raman spectroscopy provided typical Raman spectra for the studied amphiboles, highlighting distinct features such as bands related to CMg content, CFe3+ presence, TO4 ring-breathing mode, TiO6 stretching mode, presence > 0.3 apfu of CTi, and TO4 stretching indicating CFe2+ in the structure. Applied amphibole geothermobarometry revealed the formation P–T conditions of amphibole (Amp)1 (avg. 863 °C at 0.23 GPa), Amp2 (avg. 747 °C at 0.17 GPa), Amp in the mantle rocks (avg. 853 °C at 0.64 GPa), Amp5 (avg. 349 °C at 0.03 GPa), and Amp6 (avg. 694 °C at 0.46 GPa). [ABSTRACT FROM AUTHOR]

We present a reconstruction of the physicochemical conditions of melts in the Pleistocene storage and plumbing system of the Doña Juana Volcanic Complex (SW Colombia): a poorly known, potentially active polygenetic volcano of dacitic composition comprising four major edifices and showing periods of long quiescence. Compositional data for plagioclase, amphibole, pyroxene, and Fe-Ti oxides were combined with new and existing whole-rock data from representative eruptive products, allowing for the implementation of equilibrium tests and geothermobarometry calculations within an established stratigraphic, petrographic, and geochronological framework. Textural and geochemical variabilities of all mineral phases suggest the existence of a trans-crustal magmatic system feeding the Pleistocene eruptions of Doña Juana, and cyclic rejuvenation of a crystal mush following each volcano edifice collapse. The assemblage of different crystal cargos before magma recharge and final eruption is attested by (i) the coexistence of equilibrium and disequilibrium textures and variable compositions in crystals of all studied species, (ii) felsic cores in antecrysts, (iii) mafic overgrowth rims, and (iv) significantly less differentiated microcrysts relative to the composition of meso- and macrocrysts. By integrating multiple mineral-only and mineral-liquid geothermobarometers, after careful textural analyses, we estimate the intensive parameters of the mush–melt interaction zone of the plumbing system in the middle crust, providing a preliminary view of the architecture of a trans-crustal magmatic system in a complex tectonic setting at a previously understudied area of the north-Andean volcanic zone. [ABSTRACT FROM AUTHOR]

Abstract Background Asbestos lung content is regarded as the most reliable tool for causal attribution of malignant mesothelioma (MM) to previous asbestos exposures. However, there is a lack of studies on asbestos burden in lungs of MM patients in comparison with healthy individuals. This study aims to provide such a comparison, investigating, as well, differences in asbestos lung burden with sex and time trends. Methods Asbestos lung content has been assessed on formalin-fixed lung fragments using scanning electron microscopy coupled with energy dispersion spectroscopy (SEM–EDS) on individuals deceased from MM (cases) and healthy subjects without any lung disease who died from violent causes (controls) between 2005 and 2023. Results Asbestos and asbestos bodies (ABs) were found, respectively, in 73.7% and 43.2% of cases and in 28 and 22% of controls; in MM cases the most represented asbestos types were crocidolite and amosite, whereas in controls it was tremolite-actinolite asbestos. The concentration of both asbestos fibers and ABs was statistically significantly higher in MM cases compared to controls. The mean asbestos fibers width was also significantly higher in cases than controls. Males and females with MM showed similar asbestos and ABs concentrations, but females had higher concentrations of chrysotile, and significantly lower fibers width compared to males. Time trends show that MM lung asbestos concentrations decreased starting in 2011. Discussion The results suggest a correlation between asbestos burden in lungs and MM risk. The different concentration of chrysotile, as well as the different width of asbestos fibers in MM males and females might reflect a sex difference in response of the lung microenvironment to inhaled asbestos. Finally, this study provides the first pathological evidence of the effect of the ban of asbestos use, demonstrating a significant decrease of asbestos lung content after 2011.

Five layers of detrital amphiboles in the CJ08-008 sediment core from the northwest Indian Ocean have been found. To analyze their genetic types and provenance, an electron probe microanalysis of 300 amphibole grains from the core was conducted to calculate the numerical and characteristic values of cations in the crystal structure. The results showed that amphiboles with high Si, Ca, and Mg contents and low Na and K contents exhibit a low degree of weathering and that amphiboles mainly comprise tschermakite (46.43~70.69%), followed by magnesiohornblende, in the calcic amphibole subgroup. The types of sources for these amphiboles are mainly different types of metamorphic and magmatic rock. A large proportion of the detrital amphiboles (>60%) are derived from metamorphic rocks, followed by intermediate acid-intrusive rocks. The genetic analysis of amphiboles showed that most of the medium acid-intrusive amphiboles belong to the crust–mantle type, followed by the mantle type. Most of the amphiboles of metamorphic origin are of the low-pressure type. The amphiboles in the CJ08-008 sediment core exhibit characteristics different from those brought by monsoons from surrounding land masses. The variations in the amphiboles indicate different sources, which may have different origins; these origins could include the Carlsberg Ridge, the Owen Fault Zone, or older submarine sediment sequences eroded by turbidity currents.

Abstract Background Asbestos is a mineral present in nature and it has been used for years in numerous settings. Asbestos enters the bloodstream and lymphatic system mainly through breathing. Objectives Studies with asbestos fiber’s quantification in human tissues are scarce except for the lung. This article summarizes asbestos studies in some extra-abdominal tissues. Methods A scoping review of articles that quantified asbestos fibers in extra-abdominal tissues (lymph nodes, pharynx, larynx, trachea, heart) by electron microscopy (Scanning—SEM or Transmission—TEM) was performed. Results The 10 studies selected comprised 52 cases, out of whom 108 samples were analyzed. Mostly samples were lymph node tissues (102), followed by larynx (3) and myocardium (3). No studies were found that determined the presence of asbestos in the pharynx or trachea. The concentration of asbestos fibers detected in the lymph nodes was from 0.003 million fibers per gram of dry tissue (mfgdt) up to 7400 mfgdt, in the larynx the range was from 0.5 mfgdt up to 3.6 mfgdt, in myocardium no asbestos fibers were detected. Discussion The studies included were heterogeneous in terms of case and sample characteristics and analytical techniques. As subjects exposed to asbestos are often positive for fibers in thoracic lymph nodes, we suggest that whenever a human tissue sample is analyzed for asbestos presence, the relevant draining lymph node should be concomitantly studied.

Fluid inclusion microthermometry on olivines, clinopyroxenes, and amphiboles was used during a volcanic eruption, in combination with real-time seismic data and rapid petrographic observations, for petrological monitoring purposes. By applying this approach to the study of 18 volcanic samples collected during the eruption of Tajogaite volcano on La Palma Island (Canary Islands) in 2021, changes in the magma system were identified over time and space. Magma batches with distinct petrographic and geochemical characteristics emerged from source zones whose depth progressively increased from 27 to 31 kilometers. The rise of magma of deeper origin is attested by fluid inclusions made of N2 and CO, markers of mantle outgassing. Magma accumulation occurred over different durations at depths of 22 to 27 and 4 to 16 kilometers. Time-integrated magma ascent velocities (including ponding times) were estimated at between 0.01 and 0.1 meters per second. This method is cost-effective and quickly identifies changes in the magma system during an eruption, enhancing petrological monitoring procedures. [ABSTRACT FROM AUTHOR]

Silicic magma reservoirs are responsible for producing the largest explosive eruptions in the geologic record. Petrologic and geochronological data provide evidence for these systems spending substantial periods of time (104–105 yrs) within the upper crust prior to eruption; however, the long-term thermochemical evolution of these systems is not fully understood, as existing petrologic data make it challenging to quantify the time interval a magmatic system has spent at certain temperatures, or its "thermal history". Here, we investigate the 74 ka Youngest Toba Tuff (YTT), one of the largest explosive eruptions in the geologic record, to better constrain the long-term thermal evolution of its magmatic system. We combine forward models of Sr diffusion in plagioclase and hornblende, mineral thermometry, and pre-existing trace-element evolution models to quantify the thermochemical evolution of the YTT magmatic system. We find that plagioclase crystals record decades to centuries of storage at temperatures > ∼ 750 ∘ C, while hornblende records up to 6200 years at the same temperatures. Hornblende crystallizes at temperatures around 820 ∘ C and adjusting our diffusion modeling to this temperature results in no more than 900 years at initial crystallization conditions. Combined with previous trace-element modeling work, these results indicate that although there was chemical diversity for long durations in the YTT magma system sufficient to produce unique composition eruptive products, the entire system was experiencing a relatively similar thermal history that did not allow for large bodies of eruptible magma to be present for long periods ( > > 102–103 years). Rather, we suggest that magmas within the YTT magmatic system were stored for long durations at thermal conditions where they were uneruptible and only remobilized within a few centuries prior to eruption. [ABSTRACT FROM AUTHOR]

Orthoamphibole, clinoamphibole and magnetite are common minerals in altered rocks associated spatially with Palaeoproterozoic volcanogenic massive sulfide (VMS) deposits in Colorado, USA and metamorphosed to the amphibolite facies. These altered rocks are dominated by the assemblage orthoamphibole (anthophyllite/gedrite)–cordierite–magnetite±gahnite±sulfides. Magnetite also occurs in granitoids, banded iron formations, quartz garnetite, and in metallic mineralisation consisting of semi-massive pyrite, pyrrhotite, chalcopyrite, and sphalerite with subordinate galena, gahnite and magnetite; amphibole also occurs in amphibolite. The precursor to the anthophyllite/gedrite–cordierite assemblages was probably the assemblage quartz–chlorite formed from hydrothermal ore-bearing fluids (~250° to 400°C) associated with the formation of metallic minerals in the massive sulfide deposits. Element–element variation diagrams for amphibole, magnetite and ilmenite based on LA-ICP-MS data and Principal Component Analysis (PCA) for orthoamphiboles and magnetite show a broad range of compositions which are primarily dependent upon the nature of the host rock associated spatially with the deposits. Although discrimination plots of Al/(Zn+Ca) vs Cu/(Si+Ca) and Sn/Ga vs Al/Co for magnetite do not indicate a VMS origin, the concentration of Al+Mn together with Ti+V and Sn vs Ti support a hydrothermal rather than a magmatic origin for magnetite. Principal Component Analyses also show that magnetite and orthoamphibole in metamorphosed altered rocks and sulfide zones have distinctive eigenvalues that allow them to be used as prospective pathfinders for VMS deposits in Colorado. This, in conjunction with the contents of Zn and Al in magnetite, Zn and Pb in amphibole, ilmenite and magnetite, the Cu content of orthoamphibole and ilmenite, and possibly the Ga and Sn concentrations of magnetite constitute effective exploration vectors. [ABSTRACT FROM AUTHOR]

The utilisation of plant-based temper in Songze culture pottery incorporated a substantial proportion of fibre and exhibited a microstructure resembling a fully oxidised rice husk temper (Grog). However, during the Liangzhu and Guangfulin periods, these plant-based tempers underwent a transformation into quartz and other mineral tempers. Notably, amphibole tempers were identified in pottery from the Liangzhu culture, particularly in black pottery coatings. The structure of the low-aluminium ceramic coating was determined to be porous, and initially, this type of temper was thought to be debris resulting from jade processing. However, experimental archaeological studies have demonstrated that it is difficult for jade fragments to develop a similar petrographic structure. In pottery from the Guangfulin culture, white pottery coatings turned black when compacted. This colour alteration may have been achieved through simple sintering processing, suggesting the potential utilisation of a two-step pottery processing technique under low-fire conditions. [ABSTRACT FROM AUTHOR]

Large swaths of juvenile crust with tonalite-trondhjemite-granodiorite (TTG) composition were added to the continental crust from about 3.5 billion years ago. Although TTG magmatism marked a pivotal step in early crustal growth and cratonisation, the petrogenetic processes, tectonic setting and sources of TTGs are not well known. Here, we investigate the composition and petrogenesis of Archaean TTGs using high field-strength-element systematics. The Nb concentrations and Ti anomalies of TTGs show the overwhelming effects of amphibole and plagioclase fractionation and permit constraints on the composition of primary TTG melts. These melts are relatively incompatible element-poor and characterised by variably high La/Sm, Sm/Yb and Sr/Y, and positive Eu anomalies. Differences in these parameters are not indicative of melting depth, but instead track differences in the degree of melting and fractional crystallisation. Primary TTGs formed by the melting of rutile- and garnet-bearing plagioclase-cumulate rocks that resided in proto-continental roots. The partial melting of these rocks is part of a causal chain that links TTG magmatism to the formation of sanukitoids and K-rich granites. Together, these processes explain the growth and differentiation of the continental crust during the Archaean without requiring external forcing such as meteorite impact or the start of global plate tectonics. Earth's early continental crust formed by the melting of plagioclase-cumulates. Melting of these rocks, and subsequent crustal delamination and remelting, can explain the growth and differentiation of the continental crust during the Archaean. [ABSTRACT FROM AUTHOR]

Amphibole asbestos is related to multiple diseases, mainly those targeting the lungs. Asbestos-related malignancies can also be caused by non-regulated asbestiform minerals and some elongated mineral particles (EMPs). In particular, the role of nano- and micro-sized EMPs internalized by lung epithelial cells must be clarified. This is of major importance when considering that EMPs to which humans are exposed are likely a highly heterogeneous mix of different mineral types, shapes, and sizes. Here, we document that particles smaller than 4.54 µm in length and smaller than 0.89 µm in width (e.g., particles that do not fit the regulatory categories to be identified as asbestos) are easily internalized because of their specific dimensions, surface charge, and shape (mostly dictated by the aspect ratio L/w). Once internalized, these particles can be found in proximity to the cell nucleus, in vesicles, and in the cytoplasm. Examining the localization of particles in cells provides important information, which helps in determining the physicochemical environment found inside the biological compartment, thus allowing for a better comprehension of the mineralogical transformation that might happen after internalization by cells. [ABSTRACT FROM AUTHOR]

Amphiboles in the upper mantle (most frequently pargasitic in composition) have recently gained attention due to their role in the water budget and potential control on the rheology and physical discontinuity of layers of the mantle. Although nominally anhydrous minerals are often analyzed with Fourier transform infrared (FTIR) spectroscopy, amphiboles, especially in natural samples, are only rarely the focus of such studies because of their complex structure and variable composition. In mantle xenoliths, amphibole occurs not only interstitially or forming veins, but also as lamellae within orthopyroxene and/or clinopyroxene grains. The genesis of such lamellae is often ambiguous, as they could either be meta-somatic products, or form by exsolution without an external H2O source upon decreasing P-T conditions and consequent destabilization of hydrous point defects in the host pyroxene. To constrain the origin of amphibole lamellae in pyroxenes, we studied mantle xenoliths from the Carpathian-Pannonian region (CPR) by applying hyperspectral imaging using an FTIR equipped with focal plane array (FPA) detector. Amphibole lamellae are absent in xenoliths of the central part of the CPR, but appear in those from the marginal localities that represent a well-hydrated supra-subduction mantle environment. Some of the lamella-hosting pyroxene grains are in contact with interstitial amphibole, suggesting that the formation of the lamellae is related to the amphibole-producing metasomatism; however, others have no adjacent amphibole. To determine the origin of the amphibole lamellae in pyroxenes without neighboring amphibole, hyperspectral images were used to give an estimation of their volume proportion (0.8–5.1 vol%) in the pyroxenes. Using these volume proportions, we calculated that a bulk water content of ~330–670 (orthopyroxene) and ~740–1430 (clinopyroxene) wt. ppm is needed to be contained in the host grain to be able to facilitate subsolidus exsolution of the observed amount of amphibole lamellae. These water contents are, however, too high for mantle pyroxenes, even for an aqueous-fluid saturated upper mantle. This suggests that the formation of amphibole lamellae is related to a metasomatic event with fluid input from an external water source (e.g., melt/fluid inclusion or metasomatic agent on the grain boundary). [ABSTRACT FROM AUTHOR]

Scandian actinolite evolving to scandio-winchite (up to 5.45 wt% Sc2O3) has been found in chloritedominant xenoliths incorporated into marginal portion of a granitic pegmatite. The pegmatite intruded a blackwall schist zone developed around rodingite-type rocks exposed in a serpentinite quarry at Jordanów Śląski near Sobótka, ~30 km south of Wrocław, Lower Silesia, Poland. The amphiboles form irregular overgrowths around cascandite and represent a complex solid-solution series among actinolite and scandio-winchite end-members, with a trace contribution of "scandio-magnesio-hornblende." Structural studies of a scandian actinolite crystal with composition A[□0.995(2)K0.005(2)]Σ1B[Na0.24(5)Ca1.73(4)]Σ1.98(1) C M g 3.74 (7) F e 0.90 (3) 2 + M n 0.04 (1) S c 0.26 (3) A l 0.05 (1) Σ 4.99 (1) T S i 7.98 (2) A l 0.02 (2) Σ 8.00 O 22 (O H) 2 revealed monoclinic C2/m structure with unit-cell parameters a = 9.8517(3), b = 18.0881(6), c = 5.28501(18) Å, β = 104.809(4)°, in which scandium is located solely at the CM2 site. Scandian amphiboles are uncommon in geological environments, and invite comments on the origin of the observed Sc enrichment in the amphibole structure. Textural appearance of the chlorite-cascandite-amphibole clusters suggests that the formation of the amphiboles is related to the evolution of the country rocks followed by partial alteration of blackwall schist xenoliths by pegmatite-forming melt. [ABSTRACT FROM AUTHOR]

Compositional variations of amphibole stratigraphically recovered from multiple eruptions at a given volcano have a great potential to archive long-term magmatic processes in its crustal plumbing system. Calcic amphibole is a ubiquitous yet chemically and texturally diverse mineral at Mount St. Helens (MSH), where it occurs in dacites and in co-magmatic enclaves throughout the Spirit Lake stage (last ~4000 years of eruptive history). It forms three populations with distinct geochemical trends in key major and trace elements, which are subdivided into a high-Al (11–14.5 wt% Al2O3), a medium-Al (10–12.5 wt% Al2O3), and a low-Al (7.5–10 wt% Al2O3) amphibole population. The oldest investigated tephra record (Smith Creek period, 3900–3300 years BP) yields a bimodal amphibole distribution in which lower-crustal, high-Al amphibole cores (crystallized dominantly from basaltic andesite to andesite melts) and upper-crustal, low-Al amphibole rims (crystallized from rhyolitic melt) document occasional recharge of a shallow silicic mush by a more mafic melt from a lower-crustal reservoir. The sudden appearance of medium-Al amphiboles enriched in incompatible trace elements in eruptive periods younger than 2900 years BP is associated with a change in reservoir conditions toward hotter and drier magmas, which indicates recharge of the shallow silicic reservoir by basaltic melt enriched in incompatible elements. Deep-crystallizing, high-Al amphibole, however, appears mostly unaffected by such incompatible-element-enriched basaltic recharge, suggesting that these basalts bypass the lower crustal reservoir. This could be the result of the eastward offset position of the lower crustal reservoir relative to the upper crustal storage zone underneath the MSH edifice. Amphibole has proven to be a sensitive geochemical archive for uncovering storage conditions of magmas at MSH. In agreement with geophysical observations, storage and differentiation have occurred in two main zones: an upper crustal and lower crustal reservoir (the lower one being chemically less evolved). The upper crustal silicic reservoir, offset to the west of the lower crustal reservoir, has captured compositionally unusual mafic recharge (drier, hotter, and enriched in incompatible trace elements in comparison to the typical parental magmas in the region), resulting in an increased chemical diversity of amphiboles and their carrier intermediate magmas, in the last ~3000 years of MSH's volcanic record. [ABSTRACT FROM AUTHOR]

Fudge dikes of diorite and microdiorite are penetrated in the Mio-Pliocene sedimentary-volcanic series in the northeast of Bam. In terms of lithology, these dikes are placed in two categories: gabbro-diorite. The primary minerals of the dikes are plagioclase, amphibole (hornblende), and augite, and secondary minerals such as chlorite, biotite, and sericite. Also, their textures are granular, ophitic, and microgranular. From the geochemical point of view, gabbro-diorites have sub-alkaline and met aluminum with enrichment of LILE and HREE and depletion of Nb and Ta elements. The parental magma of the gabbro-diorites is obtained from the melting of a part of the subcontinental lithospheric mantle affected by the subduction producers and in equilibrium with lherzolite spinel. The characteristics of incompatible element patterns include LILE enrichment and HFSE depletion compared to REE similar to subduction zone igneous rocks. These rocks show the intermediate geochemical characteristics of the volcanic arc magmatism of arc islands and margins, consistent with the formation of these rocks in active continents. Geochemical evidence, as well as the association of igneous rocks with green tuffites and other shallow sea sediments, indicate the occurrence of an extensional basin behind the continental arc. [ABSTRACT FROM AUTHOR]

Ultra-depleted peridotites have been reported from the mantle sections of a number of ophiolitic complexes (e.g., Papua New Guinea and New Caledonia). Such rocks are residues derived from boninitic melts in supra-subduction zones, particularly in forearcs. In the mantle wedge, slab-derived fluid-melt containing H2O increases the degree of melting and metasomatizes the peridotites. However, the relationship between high-degree melting under hydrous conditions and metasomatism is not well understood. In this paper, we report petrological features of amphibole-bearing ultra-depleted peridotites from the Horokanai ophiolite, Hokkaido, Japan. The peridotite complex in the Horokanai ophiolite consists of clinopyroxene-free harzburgite, orthopyroxene-poor harzburgite, and dunite. The harzburgites contain high-Cr# spinel (0.70-0.85) and orthopyroxene with very low abundances of incompatible elements (e.g., Y < 0.01 μg/g; Ti ~ 2 μg/g). Pargasitic-edenitic amphibole occurs as spinel-hosted inclusions and as an interstitial phase to olivine and orthopyroxene. The harzburgite is a residue formed by the high-degree melting caused by fluid flux. The hydrous conditions cause incongruent melting of orthopyroxene, producing a depleted Si-rich melt (i.e., a boninitic melt). Because such Si-rich melt can coexist with Cr-rich spinel under these conditions, amphibole is ultimately crystallized in the harzburgite. Such amphibole formation is important in producing secondary sodic amphibole during alteration of ultra-depleted peridotites. [ABSTRACT FROM AUTHOR]

The study of noble metal minerals of the Ural–Alaskan-type (UA-type) complexes has been traditionally focused on their platinum-bearing dunites and chromitites, while clinopyroxenites have been poorly considered. In this study, we report the first detailed data on the noble metal mineral assemblage in clinopyroxenites of the Kachkanar intrusion, which is a part of a UA-type complex and is renowned for its huge Ti-magnetite deposits. High concentrations of Pd, Au and Ag are closely linked to Cu-sulfide mineralization in amphibole clinopyroxenites, in which they form Pd-Ag-Au minerals: keithconnite Pd3−xTe, sopcheite Ag4Pd3Te4, stutzite Ag5−xTe3, hessite Ag2Te, merenskyite PdTe, kotulskite Pd(Te,Bi), temagamite Pd3HgTe, atheneite (Pd,Hg)3As, potarite PdHg, electrum AuAg and Hg-bearing native silver. Among those, six mineral phases are first reported for clinopyroxenites of the Ural platinum belt. Our evidence supports a petrological model, suggesting that during fractionation of high-Ca primitive magmas at high oxygen fugacity, Pt, Os, Ir, Ru and Rh accumulate in early olivine–chromite cumulates, while Pd, Au and Ag reside in the melt until sulfide saturation occurs and then concentrate in sulfide mineralization. Subsequently, this sulfide mineralization is likely affected by cumulate degassing, which results in a partial resorption of the sulfides and Pd, Au and Ag remobilization by fluid. Second-stage concentration of the sulfides and the chalcophile noble metals in the amphibole-rich rocks may occur when H2O from the fluid reacts with pyroxenes to form amphiboles, and the fluid becomes oversaturated with sulfides and chalcophile elements. [ABSTRACT FROM AUTHOR]

A detailed mineral-scale study was conducted on pumices of the latest, dominantly explosive eruption epoch (56–30 ka) of Ciomadul, the youngest, long-dormant volcano in eastern-central Europe for characterizing the magma storage system and for understanding better the changes in eruption style from effusive to explosive. The mineral cargo of dacitic pumices enables us to constrain the conditions of the pre-recharge crystal mush, the recharge magmas and the post-recharge magma prior to eruptions. A careful evaluation of the results yielded by various thermometers, barometers, oxybarometers, chemometers and hygrometers as well as direct comparison with experimental data were necessary to select the appropriate techniques and therefore to constrain the conditions for the Ciomadul magmatic system. Beneath the volcano, a felsic crystal mush body is inferred at 8–12 km depth comprising slightly oxidized (0.5–1.6 ∆NNO), low-temperature (680–750 °C), highly crystalline magma. This zone is underlain by a deep magma storage zone with less evolved, hot (> 900 °C) magma at 16–40 km depth. The dominantly explosive volcanism after the effusive eruptions (160–90 ka) can be explained by the ascent of distinct recharge magmas. They contained high-Mg (MgO > 18 wt%) amphibole, which could have crystallized from ultrahydrous (H2O > 8 wt%) magma at near-liquidus conditions. The rates of amphibole overgrowth and microphenocryst formation require weeks to months for the magma mixing and the eruption events. The hybridized melt became more oxidized and contained dissolved water in around 5.5 wt% at temperature of 790–830 °C calculated from the re-equilibrated Fe-Ti oxides. These magma properties along with the degree of crystallinity (27–38 vol% crystals) favored rapid magma ascent and an explosive style eruption. Thus, the strongly hydrous nature of the recharge magma in addition to the crystallinity and H2O content of the pre-eruption magma plays an important role in controlling the eruption style. [ABSTRACT FROM AUTHOR]

Mangani-eckermannite, ideally NaNa2(Mg4Mn3+)Si8O22(OH)2, is a new member of the amphibole supergroup found at Tanohata Mine, Shimohei District, Iwate Prefecture, Japan. It occurs as prismatic crystals up to 0.3 × 0.2 mm and their aggregates up to 1 mm intergrown with braunite, vittinkiite and quartz. Mangani-eckermannite is cherry-red to very dark red and reddish-brown in thicker grains. It is translucent with a pinkish white streak and vitreous lustre. It is brittle, fracture is stepped along crystal elongation and uneven across a crystal. Cleavage is perfect on {110}. Mohs hardness is 6. D meas = 3.16(2) and D calc = 3.186 g/cm3. The mineral is optically biaxial (–), with α = 1.645(3), β = 1.668(2), γ = 1.675(3) (589 nm); 2Vmeas = 60(10)°, 2Vcalc = 57°. The empirical formula derived from electron microprobe analysis, secondary-ion mass spectrometry and single-crystal structure refinement and calculated on the basis of 24 (O+OH) atoms per formula unit (apfu) is A(Na0.74K0.24□0.02)Σ1.00B(Na1.52Ca0.24Mn2+0.24)Σ2.00C(Mg2.54Mn2+1.45Mn3+0.71Fe3+0.26Ti0.04)Σ5.00T(Si7.97Al0.03)Σ8.00O22W[(OH)1.52O0.48]Σ2.00. Mangani-eckermannite is monoclinic, space group C 2/ m , a = 9.9533(4), b = 18.1440(7), c = 5.2970(2) Å, β = 103.948(4)°, V = 928.39(6) Å3 and Z = 2. The strongest lines of the powder X-ray diffraction pattern [ d , Å (I , %)(hkl)] are: 8.52(100)(110); 4.54(25)(040); 3.41(29)(131); 3.16(23)(310,201); 2.721(37)(151); 2.533(26)($\bar{2}$ 02). The crystal structure was refined to R 1 = 0.0264 for 1001 independent reflections with I > 2σ(I). The place of mangani-eckermannite in the nomenclature of the amphibole supergroup is discussed and the status of mangano-ferri-eckermannite as a valid mineral species and successor of 'kôzulite' is questioned. [ABSTRACT FROM AUTHOR]

Background: Asbestos lung content is regarded as the most reliable tool for causal attribution of malignant mesothelioma (MM) to previous asbestos exposures. However, there is a lack of studies on asbestos burden in lungs of MM patients in comparison with healthy individuals. This study aims to provide such a comparison, investigating, as well, differences in asbestos lung burden with sex and time trends. Methods: Asbestos lung content has been assessed on formalin-fixed lung fragments using scanning electron microscopy coupled with energy dispersion spectroscopy (SEM–EDS) on individuals deceased from MM (cases) and healthy subjects without any lung disease who died from violent causes (controls) between 2005 and 2023. Results: Asbestos and asbestos bodies (ABs) were found, respectively, in 73.7% and 43.2% of cases and in 28 and 22% of controls; in MM cases the most represented asbestos types were crocidolite and amosite, whereas in controls it was tremolite-actinolite asbestos. The concentration of both asbestos fibers and ABs was statistically significantly higher in MM cases compared to controls. The mean asbestos fibers width was also significantly higher in cases than controls. Males and females with MM showed similar asbestos and ABs concentrations, but females had higher concentrations of chrysotile, and significantly lower fibers width compared to males. Time trends show that MM lung asbestos concentrations decreased starting in 2011. Discussion: The results suggest a correlation between asbestos burden in lungs and MM risk. The different concentration of chrysotile, as well as the different width of asbestos fibers in MM males and females might reflect a sex difference in response of the lung microenvironment to inhaled asbestos. Finally, this study provides the first pathological evidence of the effect of the ban of asbestos use, demonstrating a significant decrease of asbestos lung content after 2011. [ABSTRACT FROM AUTHOR]