This study aims at detailed characteristics and comparison between dusts from various iron and non-ferrous metal production processes in order to identify individual mineral phases, chemical composition, and their influence on the values of magnetic susceptibility. Various analytical methods used include inductively coupled plasma optical emission spectroscopy, X-ray diffraction, scanning electron microscopy, and Mössbauer spectroscopy integrated with magnetic susceptibility measurements and thermomagnetic analysis. Metallurgical wastes that have arisen at different production stages of iron and non-ferrous steel are subjected to investigation. The analyzed dust samples from the iron and non-ferrous metallurgy differ in terms of magnetic susceptibility as well as their mineral and chemical composition. The research confirmed the presence of many very different mineral phases. In particular, interesting phases have been observed in non-ferrous dust, for example challacolloite, which was found for the first time in the dusts of non-ferrous metallurgy. Other characteristic minerals found in non-ferrous metallurgy dusts are zincite, anglesite, and lanarkite, while dusts of iron metallurgy contain mostly metallic iron and iron-bearing minerals (magnetite, hematite, franklinite, jacobsite, and wüstite), but also significant amounts of zincite and calcite.

The cause of the split of ⁴A⁴E(⁴G) Mn²⁺ excited level measured on minerals spectra is discussed. It is our view that ∆E = |4E(4G) − 4A(4G)| should be considered an important spectroscopic parameter. Among the possible reasons for the energy levels splitting taken under consideration, such as the covalent bond theory, the geometric deformation of the coordination polyhedron and the lattice site’s symmetry, the first one was found to be inappropriate. Two studied willemite samples showed that the impurities occur in one of the two available lattice sites differently in both crystals. Moreover, it was revealed that the calculated crystal field Dq parameter can indicate which of the two non-equivalent lattice sites positions in the willemite crystal structure was occupied by Mn²⁺. The above conclusions were confirmed by X-ray structure measurements. Significant differences were also noted in the Raman spectra of these willemites.

The new mineral sharyginite, Ca₃TiFe₂O₈ (P2₁ma, Z = 2, a = 5.423(2) Å, b = 11.150(8) Å, c = 5.528(2) Å, V = 334.3(3) ų), a member of the anion deficient perovskite group, was discovered in metacarbonate xenoliths in alkali basalt from the Caspar quarry, Bellerberg volcano, Eifel, Germany. In the holotype specimen, sharyginite is widespread in the contact zone of xenolith with alkali basalt. Sharyginite is associated with fluorellestadite, cuspidine, brownmillerite, rondorfite, larnite and minerals of the chlormayenite-wadalite series. The mineral usually forms flat crystals up to 100 µm in length, which are formed by pinacoids {100}, {010} and {001}. Crystals are flattened on (010). Sharyginite is dark brown, opaque with a brown streak and has a sub-metallic lustre. In reflected light, it is light grey and exhibits rare yellowish-brown internal reflections. The calculated density of sharyginite is 3.943 g·cm^-3. The empirical formula calculated on the basis of 8 O apfu is Ca_3.00(Fe³⁺_1.00Ti⁴⁺_0.86Mn⁴⁺_0.11Zr_0.01Cr³⁺_0.01Mg_0.01)_Σ2(Fe³⁺_0.76Al_0.20Si_0.04)_Σ1.00O₈. The crystal structure of sharyginite, closely related to shulamitite Ca₃TiFeAlO₈ structure, consists of double layers of corner-sharing (Ti, Fe³⁺) O₆ octahedra, which are separated by single layers of (Fe³⁺O₄) tetrahedra. We suggest that sharyginite formed after perovskite at high-temperature conditions >1000°C.

Peat sediments represent important environmental and climatic archives, as well as recording information on the processes affecting the formation of these deposits; combined these data can be used for paleoreconstruction of peat-bogs. In this paper we characterize heavy mineral-rich sandy layers from two peat-bog sites in Mizerów and Strumień (Poland). In both cases, the most common identified mineral suite is: epidote, staurolite, tourmaline (dravite and schörl), garnet, spinel, Al₂SiO₅ polymorphs (sillimanite, kyanite, andalusite), amphibole (mainly hornblende), pyroxene (e.g., richterite, diopside), perovskite, topaz, cordierite, apatite, monazite, chromite, ilmenite, chlorite, iron oxides, rutile and siderite. This mineral suite is characteristic of a metamorphic aureole surrounding a magmatic body. Pyrite is likely authigenic in origin. Apatite and monazite were employed for U-Pb and CHIME dating, respectively. Based on the U-Pb age information composition and textural features of selected minerals, different provenance areas were indicated: the Tatra Massif, the Bohemian Massif, and the Silesian Basin area. Transport of the investigated mineral phases was linked to development of both the Odra (praOdra) and the Vistula valleys.

The chalcocite group minerals are widely distributed among different hydrothermally affected rocks, the oxidized zone of copper sulfide deposits, or may be even crystalline from supersaturated volcanic gases. Some of the chalcocite group minerals form the main Cu orebodies. Djurleite (Cu₃₁S₁₆) is a rare member of the chalcocite group, with a very complex structure. The physical and chemical similarities between all members of the group make them almost unidentifiable by macroscopic and microscopic methods. In this study, Ag-bearing djurleite from the Kupferschiefer deposits, Lower Silesia, Poland, is characterized by EMPA (Electron Microprobe Analyses), XRD (X-Ray Diffraction), and Raman spectroscopy. Djurleite from the investigated site has the following general, average chemical formula: Cu_30.86Ag_0.1Fe_0.04S₁₆. The Ag content is up to 0.55 wt.%, while Fe is up to 0.19 wt.%. The presence of djurleite confirms a low-temperature (~90 °C), hydrothermal origin of the Cu-Ag deposit in Kupferschiefer, which is consistent with previously studies. Moreover, the authors believe that Ag-rich djurleite may often be mistaken for Ag-rich chalcocite, which used to be one of the main Ag-bearing minerals in the orebody from the Cu-Ag deposit in the Fore-Sudetic Monocline. However, the confirmation of such a statement requires more samples, which should be studied in detail.

Preservation of soft parts (collagen fibres, blood vessels and cells) in extinct vertebrates is rare and usually limited to fossilized bone and cartilage. Well-preserved coarse collagenous fibre bundles embedded in a mineralized matrix of tendons, as well as numerous hollow, tubular structures consistent morphologically with fibril bundles, blood vessels and associated cells, were identified in ossified tendons of Late Cretaceous ornithischians from North America and Central East Asia. Detailed, high-accuracy imaging, along with spectroscopic characterization of those fibrous structures and comparison with ossified tendons of modern-day turkeys, support the proposition that physiologically driven tendon ossification is common for avians and non-avian dinosaurs. The examined soft parts were preserved through the pathway of iron-induced crosslinking and alumino-silification, documenting a variety of pathways for the preservation of soft parts, depending on the burial environment. For the first time, the structure of dinosaur fossilized tendons is analysed in detail, revealing shared histogenetic principles with modern birds and the nature of preservation.