This research was conducted on an area of inland sands characterised by various degrees of overgrowth by vegetation and soil stabilisation. This landscape’s origin is not natural but is connected to human industrial activities dating from early medieval times, which created a powerful centre for mining and metallurgy. This study aims to identify the changes in the above- and belowground phytomass in the initial stages of succession and their influence on the chemical properties and morphology of the soil. It was found that Salix arenaria dominated in primary phytomass production in all plots tested. The amounts of this species found in each community were as follows: 8.55 kg/400 m² (algae–mosses), 188.97 kg/400 m² (sand grassland–willow), 123.44 kg/400 m² (pine–willow–mosses), 14.63 kg/400 m² (sand grassland–mosses–willow), and 196.55 kg/400 m² (willow–pine–sand grassland). A notable share of Koeleria glauca was found in the phytomass production of Plots IV (45.73 kg) and V (86.16 kg). Basic soil properties (pH, C_org, N_t), available plant elements (P), and plant nutrients (Ca, Mg, K, P, Fe) beneath the dominant plant species were examined. Soil acidity (pH) varied greatly, ranging from acidic (pH = 3.2) to weakly acidic (pH = 6.3). The content of organic carbon (C_org) in individual plots beneath the dominant species in the humus horizon ranged from 0.28% to 1.42%. The maximum contents of organic carbon and total nitrogen were found in organic (O) and organic-humus (OA) horizons. The highest Pavail content was found in organic and organic-humus horizons, ranging from 10.41 to 65.23 mg/kg, and in mineral horizons under K. glauca (24.10 mg/kg) and Salix acutifola (25.11 mg/kg). The soil features and phytomass were varied differently across individual sites, representing different stages of succession.

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.

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.

Purpose: The analysis of n-alkanes in palaeoenvironmental studies of peatlands is mainly limited to ombrogenous peatlands which are a rare feature in the environment. Using n-alkane and plant macrofossil analysis, we have tracked changes in the environment in the valley of a large Central European river. We tested the possibilities for applying such studies to low-moor bogs which are the most commonly occurring type of bog in the world. Materials and methods: Representative peat samples were taken from two profiles in a peatland located in the Vistula Valley (southern Poland), and they were analysed for the occurrence and distribution of biomarkers. The distribution of n-alkanes was determined using gas chromatography-mass spectrometry (GC–MS). The botanical composition of the samples was determined by analysis of plant macrofossil remains, and the degree of peat decomposition was also determined. Results and discussion: Samples of low-moor peat were characterised by a prevalence of medium- and long-chain n-alkane homologues, which is typical for higher plants. The variable values of the CPI, CPI _(25–31), and the C₂₃/C₂₅ ratio have provided information on the stages of formation of the Zapadź bog. The source of n-alkane differentiation is vegetation change related to palaeohydrological dynamics and palaeoenvironmental conditions within the peatland. Conclusions: We have shown that analysis of n-alkanes can be successfully used in low-moor bogs as a complement to palaeobotanical and palaeozoological methods. The bringing together of these types of research enables changes in the ecosystems of large river valleys to be tracked.

The aim of the research was to assess the quality of topsoils and stream sediments in the districts of the Katowice City of southern Poland in the Upper Silesian Industrial Agglomeration, influenced primarily by the exploitation of hard coal deposits and metallurgy. The task was carried out using indicators used to assess anthropogenic soil contamination (contamination factor CF and the Igeo geoaccumulation index), as well as ecotoxicological indicators used to determine the quality of stream sediments (Threshold Effect Concentration TEC and Probable Effect Concentration PEC). In order to indicate the most polluted areas, geochemical maps of selected elements in soil and stream sediments were developed. The material comes from the top layer of soil (0.0–0.3 m) and stream sediments located in the districts of the Katowice City. The work took into account selected potentially harmful elements (PHEs). The concentrations of elements were measured using the ICP-AES method, except for Hg (the CV-AAS method). The values of the CF and Igeo indicators allowed for the indication of high concentrations of most metals, arsenic, and sulfur in the topsoil layer, significantly exceeding the geochemical background values caused by the historical exploitation of Zn-Pb and zinc ores and ferrous metallurgy. The values of the TEC and PEC indicators classify the sediments into categories that may threaten the environment and living organisms.