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Zinc oxide (ZnO) is one of the main functional materials used to realize chemiresistive gas sensors. In addition, ZnO can be grown through many different methods obtaining the widest family of unique morphologies. However, the relationship between the ZnO morphologies and their gas sensing properties needs more detailed investigations, also with the aim to improve the sensor performances. In this work, seven nanoforms (such as leaves, bisphenoids, flowers, needles, etc.) were prepared through simple wet chemical synthesis. Morphological and structural characterizations were performed to figure out their growth mechanisms. Then, the obtained powders were deposited through screen-printing technique to realize thick film gas sensors. The gas sensing behavior was tested toward some traditional target gases and some volatile organic compounds (acetone, acetaldehyde, etc.) and compared with ZnO morphologies. Results showed a direct correlation between the sensors responses and the powders features (morphology and size), which depend on the specific synthesis process. The sensors can be divided in two behavioral classes, following the two main morphology kinds: aggregates of nanocrystals (leaves and bisphenoids), exhibiting best performances versus all tested gases and monocrystal based (stars, needle, long needles, flowers, and prisms).

New guidelines for the nomenclature of polymorphs and polysomes have been approved by the the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA-CNMNC). Several cases can be distinguished. (i) Polymorphs with different crystal systems are distinguished by the prefixes cubo- (cubic), hexa- (hexagonal), tetra- (tetragonal), trigo- (trigonal), ortho- (orthorhombic), clino- (monoclinic) and anortho- (triclinic). (ii) Polymorphs with different crystal systems but showing a pseudosymmetry should show the prefix 'pseudo-'. (iii) Polymorphs with the same crystal system but different space groups are distinguished by the prefix 'para-'. If three or more polymorphs show the same crystal system but different space groups, the space group notation may be added as a suffix, though such a nomenclature should be avoided if possible. (iv) Polymorphs with the same space group are distinguished by the prefix 'para-'. (v) Minerals with polymorph suffixes but with different chemical compositions cannot be considered as true polymorphs, so we recommend using the prefix 'meta-', which indicates a close but significantly different chemical composition. (vi) Polysomatic symbols should be placed as a suffix, which indicates the number and types of modules that alternate in the structure, such as in the högbomite supergroup, or as prefixes as in the sartorite homologous series. These recommendations have to be applied for future new mineral proposals, when the authors decide to use structural prefixes or suffixes, however modifications of historical and well-established names have to pass through the CNMNC for approval. In order to be consistent with the new guidelines, 25 mineral names are now modified: domeykite-β becomes trigodomeykite; fergusonite-(Y)-β becomes clinofergusonite-(Y); fergusonite-(Ce)-β becomes clinofergusonite-(Ce); fergusonite-(Nd)-β becomes clinofergusonite-(Nd); ice-VII becomes cubo-ice; roselite-β becomes anorthoroselite; sulphur-β becomes clinosulphur; mertieite-II becomes mertieite; mertieite-I becomes pseudomertieite; uranophane-α becomes uranophane; uranophane-β becomes parauranophane; gersdorffite-P213 becomes gersdorffite; gersdorffite-Pa3 becomes paragersdorffite; gersdorffite-Pca21 becomes orthogersdorffite; betalomonosovite becomes paralomonosovite; lammerite-β becomes paralammerite; novácekite-I becomes hydronovácekite; novácekite-II becomes novácekite; halloysite-7Å becomes halloysite; halloysite-10Å becomes hydrohalloysite; metauranocircite-I becomes metauranocircite; taimyrite-I becomes taimyrite; uranocircite-II becomes uranocircite; andorite IV becomes quatrandorite; and andorite VI becomes senandorite.

Many studies have improved our understanding of the mode of preservation at the Crato fossil Lagerstätte. The high degree of preservation of the Crato mineralized insects is thought to be a consequence of the diffusion of ions through carcasses and envelopment by bacteria that, in turn, created microenvironmental conditions that led to mineralization, mainly pyritization. Pyritized insects have been oxidized by in situ weathering to more stable oxide/hydroxy minerals during Quaternary time. This transformation is essential to maintain the palaeontological information acquired during microbially induced pyritization in an oxidizing atmosphere. However, intense weathering can diminish or obscure the morphological fidelity, and little attention has been paid to the post-diagenetic processes experienced by these fossils. Here, we aim to determine the degree of alteration undergone by Crato pyritized insects using the following combination of analytical tools: scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared and Raman spectroscopy. Our results show that well-preserved insects are preferentially replaced by haematite and poorly preserved fossils are replaced by goethite. In addition, we recorded three types of post-diagenetic alteration: insects with iron-oxide overgrowths; insects associated with black coatings, sometimes with the formation of dendrites; and insects preserved as an impression, where only the outline of the body remains. All of these alterations have the potential to distort or tarnish palaeontological information. Here, we measured the effects of such telodiagenetic alterations at macro and micro scales. Therefore, this taphonomic approach has wide applicability wherever fine-grained deposits bearing mineralized insects are found.

The paragenesis and composition of bavenite-bohseite were investigated in fifteen granitic pegmatites from the Bohemian Massif, Czech Republic. Three types distinct in their relation to primary Be precursors, mineral assemblages, morphology and origin were recognised: (1) primary hydrothermal bavenite-bohseite crystallised in miarolitic pockets from residual pegmatite fluids; and secondary bavenite-bohseite in two distinct types: (2) a proximal type restricted spatially to pseudomorphs after a primary Be mineral (beryl > phenakite, helvine-danalite); and (3) a distal type on brittle fractures and fissures of host pegmatite. The mineral assemblages are highly variable: (1) axinite-(Mn), smectite, calcite and pyrite; (2) bertrandite, milarite, secondary beryl, bazzite, K-feldspar, muscovite-illite, scolecite, gismondine-Ca, analcime, chlorite; and (3) muscovite, albite, quartz, epidote, pumpellyite-(Mg), pumpellyite-(Fe3+), titanite and chlorite. Electron microprobe analyses showed, in addition to major constituents (Si, Ca and Al), minor concentrations (in apfu) of Na (≤0.24), Fe (≤0.10), Mn (≤0.10) and F (≤0.36). The type 1 hydrothermal miarolitic bavenite-bohseite is mostly Al-rich (2.00-0.67 apfu) relative to type 2 proximal bavenite-bohseite and bohseite after beryl, phenakite and helvine-danalite (1.56-0.46, 0.70-0.05, 1.02-0.35 apfu, respectively); and type 3 distal bavenite-bohseite typically after beryl (1.63-0.09 apfu). Raman spectroscopy revealed that the distance between the OH- vibrational modes decreases with increasing bohseite component. The Al content of secondary type 2 proximal bavenite-bohseite is controlled by the composition of the Be precursor whereas type 3 distal bavenite-bohseite with beryl as the Be precursor is more variable and the composition is governed mainly by the composition of fluids. Calcium, a crucial component for bavenite-bohseite origins, was derived from residual pegmatite fluids (Vlastějovice, Vepice IV or Trebíc Plutons) or external sources (e.g. Drahonín IV, Věžná I or Marsíkov). Primary type 1 hydrothermal bavenite-bohseite from miarolitic pockets might have crystallised at T ≈ 300-400°C and P ≈ 200 MPa, whereas the secondary type 2 and 3 bavenite-bohseite formed at T ≈ 300-100°C and P ≈ 200-20 MPa.

Eclogite-facies mineral assemblages are commonly preserved in mafic protoliths within continental terranes. It is widely accepted that the entirety of these continental terrains must also have been subducted to eclogite-facies conditions. However, evidence that the felsic material transformed at eclogite-facies conditions is lacking. Low-strain metagranites of the ultrahigh-pressure metamorphic Tso Morari Complex in Ladakh, Himalaya, are host to eclogite-facies mafic sills and preserve evidence of subduction to eclogite-facies conditions. Following the eclogite-facies metamorphism, the granites and their gneissic equivalents were overprinted by amphibolite-facies Barrovian metamorphism, obscuring their earlier metamorphic history. We present evidence that the Tso Morari metagranites preserve a complex magmatic, hydrothermal and polymetamorphic history that involved four stages. Stage 1 was magmatic crystallisation, a record of which is preserved in the primary igneous mineralogy and relict igneous microstructures. Monazite grains record a U-Pb age of 474.0 ± 11.6 Ma, concurrent with a published zircon crystallisation age. Stage 2 represents pervasive late-magmatic hydrothermal alteration of the granite during emplacement and is evident in the mineral composition, particularly in the white micas preserved in the igneous domains. Stage 3 involved the (ultra)high-pressure metamorphism of these granite bodies during the Himalayan subduction of continental material. The high-pressure stage of the metamorphic history (>25 kbar at 550-650°C) is preserved as thin coronas of garnet and phengite around igneous biotite, garnet with kyanite inclusions in pseudomorphs after cordierite, and rare palisade quartz textures after coesite. Stage 4 was a result of Barrovian metamorphism of the Tso Morari Complex and is evident in the replacement of garnet by biotite. Many of these features are preserved in localised textural domains in the rock, where local equilibrium was important and the anhydrous conditions limited reaction progress, though aided preservation potential. Collectively, these four stages record a 480 Myr history of metamorphism and reworking of the northernmost Indian plate.

Mineral replacement reactions are common in the various environments where rocks have undergone re-equilibration with geologic fluids. Replacement reactions commonly take the form of fluid-aided, coupled dissolution-precipitation and often result in pseudomorph formation. One class of environment that frequently shows significant examples of mineral replacements is hydrothermal ore deposit systems. The goal of this study was to test the simultaneous reactivity of fluorapatite and monazite in Na- and Si-rich hydrothermal fluids, which partially mimic the mineralogy and fluid chemistry of the Llallagua tin deposit in Bolivia. A series of experiments were performed at 300 to 600°C and 100 MPa, utilizing various combinations of monazite, fluorapatite, and H2O+Na2Si2O5 Reaction products were evaluated using scanning electron microscopy, electron microprobe analysis, and single-crystal X-ray diffraction. The results of this experimental study show that fluorapatite and monazite are differentially reactive under the conditions studied. The reaction products, pathways, and kinetics have a large temperature dependence. The 300 and 400°C experiments show variable amounts of monazite replacement and only minor, if any, dissolution or reactivity of fluorapatite. The high-temperature 500 and 600°C experiments are characterized by massive replacement of monazite by vitusite and britholite. Exclusively at 600°C, monazite alteration takes the form of symplectite development at the reaction front as vermicular intergrowths of vitusite and britholite. The higher-temperature experiments also show substantially more reactivity by fluorapatite, which is partially pseudomorphically altered into britholite. This is an example of regenerative mineral replacement where both fluorapatite and britholite share the same atomic structure and are crystallographically coherent after the partial replacement. The britholite replacement is characterized by the presence of oriented nanochannels, which facilitate fluid-based mass transfer between the bulk solution and the reaction front. The fluorapatite replacement is enhanced by monazite alteration through a self-perpetuating, positive feedback mechanism between these two reactions, which enhance the REE mobility in alkali-bearing fluids and further drives bulk re-equilibration. These results have potential geochronologic implications and may be significant in the evaluation of monazite and fluorapatite as potential solid nuclear waste forms. They also give us deeper insights into the mechanism of mineral replacement reactions and porosity development.

Glendonites are pseudomorphs of the mineral ikaite (CaCO3·6H2O) after loss of hydration water and occur in distinctive euhedral crystalline forms, sometimes clustered as rosettes of up to tens of centimeters in diameter. While it is generally accepted that organic-rich environments, methane seeps, and high phosphate levels are important for ikaite formation, glendonite occurrences in ancient sedimentary sequences are widely considered to reflect near-freezing temperatures, even at high latitudes during periods of greenhouse climates. To fully understand the paleoenvironmental significance of glendonites, a comprehensive examination of the modern ikaite setting is necessary. Temperature is the most important parameter that has been quantitatively constrained for the presence of ikaite. Low bottom-water temperature, while a required condition for formation of the mineral, is not adequate for its growth; other controls are necessary to explain the absence of ikaite in many cold environments. In this study, we discuss the control of carbonate chemistry on ikaite formation. Our compilation of geochemical data from sediment cores with well-preserved ikaite provide further evidence for the importance of phosphate. A phosphate concentration above ∼400 μM in shallow and cold porewater may be the requisite parameter for extensive ikaite precipitation. Thus, abundant glendonites in ancient successions mark past periods and regions of elevated porewater phosphorus concentrations, which may also be related to high surface productivity and/or iron fertilization.

Plumbogaidonnayite, ideally PbZrSi3O9·2H2O, is a new gaidonnayite-group mineral discovered as a secondary product derived from the alteration of eudialyte from the Saima alkaline complex, China. It occurs as aggregates (up to 1 mm) composed of subhedral to anhedral or platy crystals (individually 5-50 µm), associated closely with microcline, natrolite, aegirine, gaidonnayite, georgechaoite, zircon, bobtraillite and britholite-(Ce) in eudialyte pseudomorphs. The crystals are transparent, colourless or light brown with a vitreous lustre. Plumbogaidonnayite is brittle with conchoidal fracture, and it has a Mohs hardness of ∼5 and a calculated density of 3.264 g/cm3. It is optically biaxial (+) with α = 1.61(3), β = 1.63(3) and γ = 1.66(4). The calculated 2V is 80°, with the optical orientations X, Y and Z parallel to the crystallographic a, b and c axes, respectively. The empirical formula is (Pb0.70Ca0.17Ba0.01K0.11Na0.01Y0.01)Σ1.01(Zr1.00Hf0.01Ti0.01 )Σ1.02Si3.01O9·2H2O calculated on the basis of nine oxygen atoms per formula unit and assuming the occurrence of two H2O groups. Plumbogaidonnayite is orthorhombic, P21nb, a = 11.7690(4) Å, b = 12.9867(3) Å, c = 6.66165(16) Å, V = 1018.17(5) Å3 and Z = 4. The nine strongest lines of its powder XRD pattern [d in Å (I, %) (hkl)] are: 6.489 (36) (020), 5.803 (100) (101), 4.661 (27) (021), 4.336 (29) (121), 3.640 (30) (221), 3.114 (79) (112), 2.947 (27) (400), 2.622 (27) (241) and 2.493 (27) (312). Plumbogaidonnayite has a similar spiral chain framework structure with gaidonnayite and georgechaoite, which is composed of SiO4 tetrahedra and ZrO6 octahedra, but with disordered extra-framework sites (cations and H2O groups) characterised by the substitution of 2Na+(K+) → Pb2+(Ca2+) + ∎ (vacancy). The discovery of plumbogaidonnayite adds a new perspective on the cation ordering and heterovalent substitution mechanism in gaidonnayite-group minerals.

A rare polygonal gold assemblage from the Bodaibo mining district (Russia) was analyzed in this study. It resembles cubic native gold from the same area described as a gold pseudomorph after pyrite. The polygonal assemblage differs from these cubic gold samples by the absence of striations, its stepped morphology, and the presence of euhedral pyrite. It was analyzed with non-destructive techniques (SEM, VSI, and X-ray CT) in order to preserve the integrity of this exceptional sample. The experimental data allowed us to understand how this rare sample could be formed. A formation of secondary deposits, i.e., eluvial placers, is compatible with the mobilization and precipitation of gold by surface effects on primary pyrite, as well as oxidation episodes producing iron oxides/hydroxides. The redox condition in the geological environment caused the pyrite dissolution and release of gold in its structure, leading to the formation of a thin layer of gold on pyrite by epitaxy rather than pseudomorphism.

We quantify the metamorphic pressure-temperature (P-T) conditions for a newly discovered silica-undersaturated high-pressure granulite (HPG) from the Central Maine Terrane (CMT) in northeastern Connecticut, U.S.A. The rocks lie within the Acadian-Neoacadian orogenic belt (Devonian) and form part of the Brimfield Schist. The Brimfield and the adjacent Bigelow Brook Formation contain silica-saturated rocks that have previously been shown to have undergone ∼1000 °C metamorphism. The pressure was less well constrained at ≥ ∼1 GPa. Silica-undersaturated rocks hold underutilized potential for pinpointing peak metamorphic conditions, particularly pressure, because of their resilience to melting and the variety of refractory minerals they contain. The typical silica-undersaturated mineral assemblage is garnet + spinel + corundum + plagioclase + K-feldspar + biotite + ilmenite. Leucosomes are syenites consisting of two feldspars ± biotite. Plagioclase is commonly antiperthitic, particularly in feldspathic domains surrounding peritectic garnet; such garnet crystals reach ∼10 cm in diameter. Alkali feldspars are perthitic. The rocks contain remarkable ellipsoidal spinels as much as 5.5 cm long comprising discrete crystallographic domains hosting crystallographically oriented lamellae of a Fe-Ti phase, most likely ilmenite. Corundum is usually colorless, but can also be found as sapphire in shades of pink, purple, and blue, particularly in antiperthite-rich domains surrounding large garnets. Some sapphires are concentrically color zoned. We carried out a P-T estimation using ternary feldspar reintegration thermometry of metamorphic antiperthites together with pseudosection modeling. Samples texturally and chemically record near-eclogite facies equilibration at minimum conditions of ∼1040 °C and ∼1.8 GPa, establishing the CMT in northeastern CT as the first known HPG locality in the U.S. These results are consistent with high P2O5 levels found in garnet (0.18 wt%), Ti-in-biotite thermometry, regional sillimanite pseudomorphs after kyanite, and preliminary experimental work on melt inclusions in garnet (Ferrero et al. 2017). The leucosomes provide strong evidence that partial melting of silica-undersaturated rocks at HPG conditions can produce syenitic magmata. Strongly melt-depleted silica-undersaturated rocks may also be protoliths for garnet + spinel + corundum xenoliths reported from kimberlites. The presence of HPG gneisses demonstrates that the large-scale thrusts of the CMT sample the deepest roots of the orogenic belt (60-70 km), and perhaps even deeper subduction zone lithologies as well.